Generic Name: Doxepin (DOX-e-pin)
Brand Name: Zonalon

Zonalon Cream is used for:

Relieving moderate itching caused by certain skin conditions.

Zonalon Cream is an antipruritic cream. It is not known exactly how it works. It may block histamine to relieve itching.

Do NOT use Zonalon Cream if:

• you are allergic to any ingredient in Zonalon Cream
• you have certain prostate problems (eg, asymptomatic prostatic hypertrophy), uncontrolled glaucoma, or trouble urinating (urinary retention)
• you are taking clonidine, an H₁ antagonist (eg, astemizole, terfenadine), or ibutilide, or you have taken a monoamine oxidase inhibitor (MAOI) (eg, furazolidone, phenelzine, isocarboxazid) within the past 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zonalon Cream:

Some medical conditions may interact with Zonalon Cream. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have a history of heart problems, seizures (eg, epilepsy), overactive thyroid, glaucoma or increased pressure in the eyes, prostate problems (eg, benign prostatic hypertrophy [BPH]), certain blood problems (eg, porphyria), suicidal thoughts or attempts, or a history of alcohol abuse

Some MEDICINES MAY INTERACT with Zonalon Cream. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Antiarrhythmics (eg, quinidine, propafenone, flecainide), antifungal medicines (eg, fluconazole, terbinafine), carbamazepine, cimetidine, mibefradil, phenothiazines (eg, chlorpromazine, thioridazine), or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine, sertraline) because they may increase the risk of Zonalon Cream’s side effects
• Anticoagulants (eg, warfarin), clonidine, guanadrel, H₁ antagonists (eg, astemizole, terfenadine), ibutilide, sulfonylureas (eg, tolazamide, glipizide), sympathomimetics (eg, phenylephrine, pseudoephedrine), or tramadol because the risk of their side effects may be increased by Zonalon Cream
• Clonidine, guanadrel, guanethidine, or guanfacine because their effectiveness may be decreased by Zonalon Cream
• MAOIs (eg, furazolidone, phenelzine, isocarboxazid) because severe toxic effects may occur

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zonalon Cream may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zonalon Cream:

Use Zonalon Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Zonalon Cream is for external use only.
• Wash and completely dry the affected area. Apply a thin film to the affected area and gently rub it in.
• Wash your hands immediately after using Zonalon Cream, unless they are part of the treated area.
• Do not bandage or otherwise cover the treated area unless directed to do so by your doctor. Avoid tight-fitting clothes on the treated area.
• If you miss a dose of Zonalon Cream, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule.

Ask your health care provider any questions you may have about how to use Zonalon Cream.

Important safety information:

• Zonalon Cream may cause drowsiness. This effect may be worse if you take it with alcohol or certain medicines. Use Zonalon Cream with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Zonalon Cream will add to the effects of alcohol and other depressants. Ask your pharmacist if you have questions about which medicines are depressants.
• Limit your alcohol consumption while taking Zonalon Cream.
• Avoid getting Zonalon Cream in your eyes or on the inside of your nose or mouth.
• Use Zonalon Cream with caution in the ELDERLY; they may be more sensitive to its effects, especially drowsiness and confusion.
• Zonalon Cream should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zonalon Cream while you are pregnant. It is not known if Zonalon Cream is found in breast milk. Do not breast-feed while taking Zonalon Cream.

Possible side effects of Zonalon Cream:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Abnormal skin sensations; burning and stinging at the application site; changes in emotions; confusion; dizziness; drowsiness; dry and tight skin; dry mouth and lips; fatigue; headache; itching; swelling; taste changes; thirst.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision; rapid or pounding heartbeat; severe burning and stinging at the application site.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Zonalon Cream may be harmful if swallowed.

Proper storage of Zonalon Cream:

Store Zonalon Cream at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zonalon Cream out of the reach of children and away from pets.

General information:

• If you have any questions about Zonalon Cream, please talk with your doctor, pharmacist, or other health care provider.
• Zonalon Cream is to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zonalon Cream. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Zolmitriptan (zohl-mi-TRIP-tan)
Brand Name: Zomig ZMT

Zomig ZMT Disintegrating Tablets are used for:

Treating acute migraine headaches with or without aura (flashing lights, wavy lines, dark spots) in adults. It is not intended to prevent migraines.

Zomig ZMT Disintegrating Tablets belongs to a group of medicines called “triptans.” It works by narrowing the widened vessels thought to cause migraine headaches.

Do NOT use Zomig ZMT Disintegrating Tablets if:

• you are allergic to any ingredient in Zomig ZMT Disintegrating Tablets
• you have a history of heart disease, uncontrolled high blood pressure, or are currently taking or have taken a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the past 14 days
• you have used an ergot alkaloid (eg, ergotamine) or other “triptan” migraine medicine in the last 24 hours
• you are currently taking sibutramine
• you have migraines caused by basal arteries or hemiplegia

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zomig ZMT Disintegrating Tablets:

Some medical conditions may interact with Zomig ZMT Disintegrating Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have heart disease (or a family history of heart disease), peripheral blood vessel disease, high cholesterol, high blood pressure, or diabetes
• if you have cluster headaches
• if you have factors that could lead to heart attacks (eg, overweight, smoking) or you are a postmenopausal woman

Some MEDICINES MAY INTERACT with Zomig ZMT Disintegrating Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because they may decrease Zomig ZMT Disintegrating Tablets’s effectiveness
• Sibutramine because the risk of side effects, such as serotonin syndrome (ie, restlessness, fever, excessive sweating, confusion, twitching, and seizures which can rarely be life-threatening), may be increased
• Other serotonin agonists (eg, sumatriptan) because they may increase the risk of Zomig ZMT Disintegrating Tablets’s side effects
• Ergot alkaloids (eg, ergotamine) or MAO inhibitors (eg, phenelzine) because risk of their side effects may be increased by Zomig ZMT Disintegrating Tabletss

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zomig ZMT Disintegrating Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zomig ZMT Disintegrating Tablets:

Use Zomig ZMT Disintegrating Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• An extra patient leaflet is available with Zomig ZMT Disintegrating Tablets. Talk to your pharmacist if you have questions about this information.
• Take Zomig ZMT Disintegrating Tablets by mouth with or without food.
• It is best to use Zomig ZMT Disintegrating Tablets as soon as you notice the headache symptoms of a migraine attack.
• Additional benefit may be obtained if the patient lies down in a quiet, dark room after administering medication.
• Zomig ZMT Disintegrating Tablets are intended for the relief of acute migraine attacks. It does not prevent or reduce the number of attacks. Use Zomig ZMT Disintegrating Tablets only for acute migraine attacks.
• Open tablet blister pack with dry hands and place the tablet on the tongue. Do not try to split the tablets.
• Take the tablet immediately after removing it from its blister. Do not store the removed tablet for future use. Throw away any unused tablets or portions that have been removed from the blister pack.
• The tablet will dissolve rapidly on the tongue and can be swallowed with saliva. It is not necessary to take Zomig ZMT Disintegrating Tablets with liquid.
• If the headache returns, you can take another tablet after 2 hours. If the first dose does not relieve the migraine attack, do not take a second dose unless advised to do so by your health care provider. Do not take more than 10 mg in a 24-hour period.
• If your medicine has expired, throw it away.
• If you miss a dose of Zomig ZMT Disintegrating Tablets and you still have a headache, follow your doctor’s dosing instructions. Contact your doctor if you are unsure of what to do if you miss a dose. Do not use Zomig ZMT Disintegrating Tablets more often than prescribed. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Zomig ZMT Disintegrating Tablets.

Important safety information:

• Zomig ZMT Disintegrating Tablets may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Zomig ZMT Disintegrating Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Diabetes patients – Zomig ZMT Disintegrating Tablets may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.
• Additional monitoring of your dose or condition may be needed if you are taking oral contraceptives (birth control pills), cimetidine, or other migraine medicines.
• The long-term effects of repeated use of Zomig ZMT Disintegrating Tablets have not been studied. The safety for treating an average of more than 4 headaches in a 30 day period has not been established.
• Lab tests, including liver function, kidney function, lung function, blood pressure, fasting blood glucose, and blood cholesterol, may be performed while you use Zomig ZMT Disintegrating Tablets. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.
• Use Zomig ZMT Disintegrating Tablets with caution in the ELDERLY; they may be more sensitive to its effects.
• Zomig ZMT Disintegrating Tablets should not be used in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.
• If you are past menopause discuss the safety of using Zomig ZMT Disintegrating Tablets with your doctor or pharmacist.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zomig ZMT Disintegrating Tablets while you are pregnant. It is not known if Zomig ZMT Disintegrating Tablets are found in breast milk. If you are or will be breast-feeding while you use Zomig ZMT Disintegrating Tablets, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Zomig ZMT Disintegrating Tablets:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Abnormal skin sensations; dizziness; drowsiness; increased sensitivity to touch; nausea; pain; warm/cold sensations; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); heart attack; pounding in the chest; tightness, pain, pressure, or heaviness in jaw, neck, throat, and chest.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include severe drowsiness.

Proper storage of Zomig ZMT Disintegrating Tablets:

Store Zomig ZMT Disintegrating Tablets at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zomig ZMT Disintegrating Tablets out of the reach of children and away from pets.

General information:

• If you have any questions about Zomig ZMT Disintegrating Tablets, please talk with your doctor, pharmacist, or other health care provider.
• Zomig ZMT Disintegrating Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zomig ZMT Disintegrating Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Zolmitriptan (zohl-mi-TRIP-tan)
Brand Name: Zomig

Zomig Spray is used for:

Treating acute migraine headaches with or without aura (flashing lights, wavy lines, dark spots) in adults. It is not intended to prevent migraines.

Zomig Spray belongs to a group of medicines called “triptans.” It works by narrowing the widened vessels thought to cause migraine headaches.

Do NOT use Zomig Spray if:

• you are allergic to any ingredient in Zomig Spray
• you have a history of heart disease, uncontrolled high blood pressure, or are currently taking or have taken a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the past 14 days
• you have used an ergot alkaloid (eg, ergotamine) or other “triptan” migraine medicine in the last 24 hours
• you are currently taking sibutramine
• you have migraines caused by basal arteries or hemiplegia

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zomig Spray:

Some medical conditions may interact with Zomig Spray. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have heart disease (or a family history of heart disease), peripheral blood vessel disease, high cholesterol, high blood pressure, or diabetes
• if you have cluster headaches
• if you have factors that could lead to heart attacks (eg, overweight, smoking) or you are a postmenopausal woman

Some MEDICINES MAY INTERACT with Zomig Spray. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because they may decrease Zomig Spray’s effectiveness
• Sibutramine because the risk of side effects, such as serotonin syndrome (ie, restlessness, fever, excessive sweating, confusion, twitching, seizures, which can rarely be life-threatening), may be increased
• Other serotonin agonists (eg, sumatriptan) because they may increase the risk of Zomig Spray’s side effects
• Ergot alkaloids (eg, ergotamine) or MAO inhibitors (eg, phenelzine) because the risk of their side effects may be increased by Zomig Sprays

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zomig Spray may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zomig Spray:

Use Zomig Spray as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• An extra patient leaflet is available with Zomig Spray. Talk to your pharmacist if you have questions about this information.
• It is best to use Zomig Spray as soon as you notice the headache symptoms of a migraine attack.
• Additional benefit may be obtained if the patient lies down in a quiet, dark room after administering medication.
• Zomig Spray is intended for the relief of acute migraine attacks. It does not prevent or reduce the number of attacks. Use Zomig Spray only for acute migraine attacks.
• Avoid spraying Zomig Spray into the eyes.
• The protective cap must not be removed from Zomig Spray until you are ready to use it.
• Do NOT test the spray before use.
• Gently blow your nose, then sit down and tilt your head back slightly. Spray the prescribed dose into 1 nostril. If your headache returns, a second nasal spray may be used anytime after 2 hours of using the first dose. If you do not respond to the first nasal spray, do not use Zomig Spray a second time without first consulting your health care provider. Do not use more than a total of 10 mg of Zomig Spray in a 24-hour period.
• If your medicine has expired, throw it away.
• If you miss a dose of Zomig Spray and you still have a headache, follow your doctor’s dosing instructions. Contact your doctor if you are unsure of what to do if you miss a dose. Do not use Zomig Spray more often than prescribed. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Zomig Spray.

Important safety information:

• Zomig Spray may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Zomig Spray with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• The long-term effects of repeated use of this medication have not been studied. The safety for treating an average of more than 4 headaches in a 30-day period has not established.
• Diabetes patients – Zomig Spray may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.
• Additional monitoring of your dose or condition may be needed if you are taking oral contraceptives (birth control pills), cimetidine, or other migraine medicines.
• Lab tests, including liver function, kidney function, lung function, blood pressure, fasting blood glucose, and blood cholesterol, may be performed while you use Zomig Spray. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.
• Use Zomig Spray with caution in the ELDERLY; they may be more sensitive to its effects.
• Zomig Spray should not be used in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.
• If you are past menopause discuss the safety of using Zomig Spray with your doctor or pharmacist.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zomig Spray while you are pregnant. It is not known if Zomig Spray is found in breast milk. If you are or will be breast-feeding while you use Zomig Spray, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Zomig Spray:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Abnormal skin sensations; dizziness; drowsiness; increased sensitivity to touch; nausea; pain; warm/cold sensations; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); pounding in the chest; tightness, pain, pressure, or heaviness in jaw, neck, throat, and chest.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include severe drowsiness.

Proper storage of Zomig Spray:

Store Zomig Spray at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zomig Spray out of the reach of children and away from pets.

General information:

• If you have any questions about Zomig Spray, please talk with your doctor, pharmacist, or other health care provider.
• Zomig Spray is to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zomig Spray. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Zolpidem (zole-PI-dem)
Brand Name: Ambien CR

Zolpidem Extended-Release Tablets are used for:

Treating insomnia (trouble falling asleep or staying asleep).

Zolpidem Extended-Release Tablets are a sedative-hypnotic, or sleep medicine. It works by helping to increase certain natural chemicals in the brain that cause sleep.

Do NOT use Zolpidem Extended-Release Tablets if:

• you are allergic to any ingredient in Zolpidem Extended-Release Tablets
• you are taking sodium oxybate (GHB)

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zolpidem Extended-Release Tablets:

Some medical conditions may interact with Zolpidem Extended-Release Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have kidney or liver problems, lung or breathing problems (eg, chronic obstructive pulmonary disease [COPD], sleep apnea), myasthenia gravis, metabolism problems, heart or blood pressure problems, or very poor health
• if you have a history of mood or mental problems (eg, depression), suicidal thoughts or behaviors, or alcohol or substance abuse or addiction
• if you are a child or teenager with a history of attention deficit hyperactivity disorder (ADHD)

Some MEDICINES MAY INTERACT with Zolpidem Extended-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Ketoconazole, HIV protease inhibitors (eg, ritonavir), or sodium oxybate (GHB) because they may increase the risk of Zolpidem Extended-Release Tablets’s side effects
• Rifampin because it may decrease Zolpidem Extended-Release Tablets’s effectiveness

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zolpidem Extended-Release Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zolpidem Extended-Release Tablets:

Use Zolpidem Extended-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Zolpidem Extended-Release Tablets comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Zolpidem Extended-Release Tablets refilled.
• Take Zolpidem Extended-Release Tablets by mouth on an empty stomach at least 2 hours after a meal.
• Swallow Zolpidem Extended-Release Tablets whole. Do not break, crush, or chew before swallowing.
• Zolpidem Extended-Release Tablets works very quickly; use Zolpidem Extended-Release Tablets right before going to sleep.
• Use Zolpidem Extended-Release Tablets only when you are able to get a full night’s sleep (7 to 8 hours).
• If you miss a dose of Zolpidem Extended-Release Tablets, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. Do not take more than your total daily dose in any 24-hour period.

Ask your health care provider any questions you may have about how to use Zolpidem Extended-Release Tablets.

Important safety information:

• Zolpidem Extended-Release Tablets may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Zolpidem Extended-Release Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Zolpidem Extended-Release Tablets; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.
• When you first start taking Zolpidem Extended-Release Tablets, it may have a “carryover” effect on you the next day. Use extreme care while doing anything that requires complete alertness (eg, driving a car).
• If your symptoms do not get better within 7 to 10 days or if they get worse, check with your doctor.
• Sleep medicines may cause a special type of memory loss or amnesia. To prevent memory problems, be sure to use Zolpidem Extended-Release Tablets only when you are able to get a full night’s sleep (7 to 8 hours) before you need to be active again. Be sure to talk to your health care provider if you think you are having memory problems.
• Some patients taking Zolpidem Extended-Release Tablets have performed certain activities while they were not fully awake. These have included sleep-driving, making and eating food, making phone calls, and having sex. Patients often do not remember these events after they happen. Such an event may be more likely to occur if you use a high dose of Zolpidem Extended-Release Tablets. It may also be more likely if you drink alcohol or take other medicines that may cause drowsiness while you use these medicine. Tell your doctor right away if such an event happens to you.
• Use Zolpidem Extended-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially dizziness or drowsiness.
• Zolpidem Extended-Release Tablets should be used with extreme caution in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed. Children may be more sensitive to Zolpidem Extended-Release Tablets’s side effects, especially dizziness, headache, and hallucinations.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zolpidem Extended-Release Tablets while you are pregnant. Zolpidem Extended-Release Tablets may cause prolonged sleep in the fetus when used during the last weeks of pregnancy. Zolpidem Extended-Release Tablets are found in breast milk. If you are or will be breast-feeding while you take Zolpidem Extended-Release Tablets, check with your doctor. Discuss any possible risks to your baby.

When sleep medicines are used every night for more than a few weeks, they may lose their effectiveness to help you sleep. This is known as TOLERANCE. Sleep medicines should usually be used only for short periods of time, such as a few days and generally no longer than 1 or 2 weeks. If your sleep problems continue, contact your doctor.

When used for longer than a few weeks or at high doses, some people develop a need to continue taking Zolpidem Extended-Release Tablets. This is known as DEPENDENCE or addiction. Be sure to tell your doctor if you have been dependent on alcohol, prescription medicines, or street drugs in the past.

If you stop taking Zolpidem Extended-Release Tablets suddenly, you may have WITHDRAWAL symptoms. These may include unpleasant feelings. In more severe cases, you may have stomach and muscle cramps, vomiting, sweating, and shakiness. Seizures may rarely occur. If you take Zolpidem Extended-Release Tablets for more than 1 to 2 weeks, do not stop taking it without talking to your doctor.

Possible side effects of Zolpidem Extended-Release Tablets:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; drowsiness (including daytime drowsiness); “drugged” feeling; dry mouth; headache; muscle aches; nausea; nose or throat irritation; sluggishness; stomach upset.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the hands, legs, mouth, face, lips, eyes, throat, or tongue; unusual hoarseness); abnormal thinking; behavior changes; chest pain; confusion; decreased coordination; difficulty swallowing or breathing; fainting; fast or irregular heartbeat; hallucinations; memory problems (eg, memory loss); mental or mood changes (eg, aggression, agitation, anxiety, depression); severe dizziness; shortness of breath; suicidal thoughts or actions; vision changes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include severe drowsiness or coma.

Proper storage of Zolpidem Extended-Release Tablets:

Store Zolpidem Extended-Release Tablets at room temperature, between 59 and 77 degrees F (15 and 25 degrees C). Brief storage at temperatures up to 86 degrees F (30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zolpidem Extended-Release Tablets out of the reach of children and away from pets.

General information:

• If you have any questions about Zolpidem Extended-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.
• Zolpidem Extended-Release Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is summary only. It does not contain all information about Zolpidem Extended-Release Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Sertraline (SER-tra-leen)
Brand Name: Zoloft

Zoloft Concentrate is used for:

Treating depression or obsessive-compulsive disorder (OCD). It may be used to treat panic disorder or posttraumatic stress disorder (PTSD). It may also be used to treat premenstrual dysphoric disorder (PMDD; a severe form of premenstrual syndrome) or social anxiety disorder. It may also be used for other conditions as determined by your doctor.

Zoloft Concentrate is a selective serotonin reuptake inhibitor (SSRI). It works by restoring the balance of serotonin, a natural substance in the brain, which helps to improve certain mood problems.

Do NOT use Zoloft Concentrate if:

• you are allergic to any ingredient in Zoloft Concentrate
• you are taking or have taken a monoamine oxidase inhibitor (MAOI) (eg, phenelzine), selegiline, or St. John’s wort within the last 14 days
• you are taking a fenfluramine derivative (eg, dexfenfluramine), an H₁ antagonist (eg, astemizole, terfenadine), nefazodone, pimozide, sibutramine, or thioridazine
• you are taking disulfiram

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zoloft Concentrate:

Some medical conditions may interact with Zoloft Concentrate. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you are allergic to latex
• if you or a family member has a history of bipolar disorder (manic-depression), other mental or mood problems, suicidal thoughts or attempts, or alcohol or substance abuse
• if you have a history of seizures, heart problems, liver problems, stomach or bowel bleeding, or metabolism problems
• if you are dehydrated, have low blood sodium levels, or drink alcohol
• if you will be having electroconvulsive therapy (ECT)

Some MEDICINES MAY INTERACT with Zoloft Concentrate. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Anorexiants (eg, phentermine), fenfluramine derivatives (eg, dexfenfluramine), linezolid, MAOIs (eg, phenelzine), metoclopramide, nefazodone, selegiline, serotonin 5-HT₁ receptor agonists (eg, sumatriptan), sibutramine, St. John’s wort, or trazodone because severe side effects, such as a reaction that may include fever, rigid muscles, blood pressure changes, mental changes, confusion, irritability, agitation, delirium, and coma, may occur
• Anticoagulants (eg, warfarin), aspirin, or nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen) because the risk of bleeding, including stomach bleeding, may be increased
• Diuretics (eg, furosemide, hydrochlorothiazide) because the risk of high or low blood sodium levels may be increased
• Tramadol because the risk of seizures may be increased
• H₁ antagonists (eg, astemizole, terfenadine) or phenothiazines (eg, chlorpromazine, thioridazine) because severe heart problems, including irregular heartbeat, may occur
• Carbamazepine or cyproheptadine because they may decrease Zoloft Concentrate’s effectiveness
• Aripiprazole, clozapine, digoxin, flecainide, lithium, phenytoin, pimozide , propafenone, risperidone, tricyclic antidepressants (eg, amitriptyline), or valproate (eg, valproic acid) because the risk of their side effects may be increased by Zoloft Concentrate

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zoloft Concentrate may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zoloft Concentrate:

Use Zoloft Concentrate as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Zoloft Concentrate comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Zoloft Concentrate refilled.
• Take Zoloft Concentrate by mouth with or without food.
• Use the dropper that comes with Zoloft Concentrate to measure your dose. Ask your pharmacist for help if you are unsure of how to measure your dose.
• Zoloft Concentrate must be diluted before you take it. Mix the prescribed amount with 4 ounces (one-half cup) of water, ginger ale, lemon/lime soda, lemonade, or orange juice. Do not mix it with any other kind of liquid.
• This mixture may become slightly hazy. This is normal.
• Drink the dose immediately after mixing. Do not store mixed medicine for use at a later time.
• Taking Zoloft Concentrate at the same time each day will help you remember to take it.
• Continue to take Zoloft Concentrate even if you feel well. Do not miss any doses.
• Do not suddenly stop taking Zoloft Concentrate without checking with your doctor. Side effects may occur. They may include mental or mood changes, numbness or tingling of the skin, dizziness, confusion, headache, trouble sleeping, or unusual tiredness. You will be closely monitored when you start Zoloft Concentrate and whenever a change in dose is made.
• If you miss a dose of Zoloft Concentrate, take it as soon as possible. If it almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Zoloft Concentrate.

Important safety information:

• Zoloft Concentrate may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Zoloft Concentrate with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Do not drink alcohol while you are taking Zoloft Concentrate.
• Check with your doctor before you use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are taking Zoloft Concentrate; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.
• Several weeks may pass before your symptoms improve. Do NOT take more than the recommended dose, change your dose, or use Zoloft Concentrate for longer than prescribed without checking with your doctor.
• Children and teenagers who take Zoloft Concentrate may be at increased risk for suicidal thoughts or actions. Adults may also be affected. The risk may be greater in patients who have had suicidal thoughts or actions in the past. The risk may also be greater in patients who have had bipolar (manic-depressive) illness, or if their family members have had it. Watch patients who take Zoloft Concentrate closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.
• If your doctor tells you to stop taking Zoloft Concentrate, you will need to wait for several weeks before beginning to take certain other medicines (eg, MAOIs, nefazodone). Ask your doctor when you should start to take your new medicines after you have stopped taking Zoloft Concentrate.
• The dropper that comes with Zoloft Concentrate contains natural dry rubber. Check with your health care provider if you are allergic to latex.
• Zoloft Concentrate may rarely cause a prolonged, painful erection. This could happen even when you are not having sex. If this is not treated right away, it could lead to permanent sexual problems such as impotence. Contact your doctor right away if this happens.
• Serotonin syndrome is a possibly fatal syndrome that can be caused by Zoloft Concentrate. Your risk may be greater if you take Zoloft Concentrate with certain other medicines (eg, “triptans,” MAOIs). Symptoms may include agitation; confusion; hallucinations; coma; fever; fast or irregular heartbeat; tremor; excessive sweating; and nausea, vomiting, or diarrhea. Contact your doctor at once if you have any of these symptoms.
• Neuroleptic malignant syndrome (NMS) is a possibly fatal syndrome that can be caused by Zoloft Concentrate. Symptoms may include fever; stiff muscles; confusion; abnormal thinking; fast or irregular heartbeat; and sweating. Contact your doctor at once if you have any of these symptoms.
• Caution is advised when using Zoloft Concentrate in the ELDERLY; they may be more sensitive to its effects, especially low blood sodium levels.
• Caution is advised when using Zoloft Concentrate in CHILDREN; they may be more sensitive to its effects, especially increased risk of suicidal thoughts or actions.
• Zoloft Concentrate should be used with extreme caution in CHILDREN younger than 6 years old; safety and effectiveness in these children have not been confirmed.
• Zoloft Concentrate may cause weight changes. CHILDREN and teenagers may need regular weight and growth checks while they take Zoloft Concentrate.
• PREGNANCY and BREAST-FEEDING: Zoloft Concentrate may cause harm to the fetus if it is used during the last 3 months of pregnancy. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zoloft Concentrate while you are pregnant. It is not known if Zoloft Concentrate is found in breast milk. If you are or will be breast-feeding while you use Zoloft Concentrate, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Zoloft Concentrate:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Anxiety; constipation; decreased sexual desire or ability; diarrhea; dizziness; drowsiness; dry mouth; increased sweating; loss of appetite; nausea; nervousness; stomach upset; tiredness; trouble sleeping; vomiting; weight loss.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bizarre behavior; black or bloody stools; chest pain; confusion; decreased bladder control; decreased concentration; decreased coordination; exaggerated reflexes; fainting; fast or irregular heartbeat; fever; hallucinations; memory loss; new or worsening agitation, panic attacks, aggressiveness, impulsiveness, irritability, hostility, exaggerated feeling of well-being, restlessness, or inability to sit still; persistent or severe ringing in the ears; persistent, painful erection; red, swollen, blistered, or peeling skin; seizures; severe or persistent anxiety or trouble sleeping; severe or persistent headache; stomach pain; suicidal thoughts or attempts; tremor; unusual bruising or bleeding; unusual or severe mental or mood changes; unusual weakness; vision changes; worsening of depression.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include coma; fainting; fast, slow, or irregular heartbeat; hair loss; hallucinations; seizures; severe or persistent diarrhea, dizziness, drowsiness, nausea, or vomiting; tremor.

Proper storage of Zoloft Concentrate:

Store Zoloft Concentrate at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zoloft Concentrate out of the reach of children and away from pets.

General information:

• If you have any questions about Zoloft Concentrate, please talk with your doctor, pharmacist, or other health care provider.
• Zoloft Concentrate is to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is summary only. It does not contain all information about Zoloft Concentrate. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Zolmitriptan (zohl-mi-TRIP-tan)
Brand Name: Zomig ZMT

Zolmitriptan Disintegrating Tablets are used for:

Treating acute migraine headaches with or without aura (flashing lights, wavy lines, dark spots) in adults. It is not intended to prevent migraines.

Zolmitriptan Disintegrating Tablets belongs to a group of medicines called “triptans.” It works by narrowing the widened vessels thought to cause migraine headaches.

Do NOT use Zolmitriptan Disintegrating Tablets if:

• you are allergic to any ingredient in Zolmitriptan Disintegrating Tablets
• you have a history of heart disease, uncontrolled high blood pressure, or are currently taking or have taken a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the past 14 days
• you have used an ergot alkaloid (eg, ergotamine) or other “triptan” migraine medicine in the last 24 hours
• you are currently taking sibutramine
• you have migraines caused by basal arteries or hemiplegia

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zolmitriptan Disintegrating Tablets:

Some medical conditions may interact with Zolmitriptan Disintegrating Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have heart disease (or a family history of heart disease), peripheral blood vessel disease, high cholesterol, high blood pressure, or diabetes
• if you have cluster headaches
• if you have factors that could lead to heart attacks (eg, overweight, smoking) or you are a postmenopausal woman

Some MEDICINES MAY INTERACT with Zolmitriptan Disintegrating Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because they may decrease Zolmitriptan Disintegrating Tablets’s effectiveness
• Sibutramine because the risk of side effects, such as serotonin syndrome (ie, restlessness, fever, excessive sweating, confusion, twitching, and seizures which can rarely be life-threatening), may be increased
• Other serotonin agonists (eg, sumatriptan) because they may increase the risk of Zolmitriptan Disintegrating Tablets’s side effects
• Ergot alkaloids (eg, ergotamine) or MAO inhibitors (eg, phenelzine) because risk of their side effects may be increased by Zolmitriptan Disintegrating Tabletss

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zolmitriptan Disintegrating Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zolmitriptan Disintegrating Tablets:

Use Zolmitriptan Disintegrating Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• An extra patient leaflet is available with Zolmitriptan Disintegrating Tablets. Talk to your pharmacist if you have questions about this information.
• Take Zolmitriptan Disintegrating Tablets by mouth with or without food.
• It is best to use Zolmitriptan Disintegrating Tablets as soon as you notice the headache symptoms of a migraine attack.
• Additional benefit may be obtained if the patient lies down in a quiet, dark room after administering medication.
• Zolmitriptan Disintegrating Tablets are intended for the relief of acute migraine attacks. It does not prevent or reduce the number of attacks. Use Zolmitriptan Disintegrating Tablets only for acute migraine attacks.
• Open tablet blister pack with dry hands and place the tablet on the tongue. Do not try to split the tablets.
• Take the tablet immediately after removing it from its blister. Do not store the removed tablet for future use. Throw away any unused tablets or portions that have been removed from the blister pack.
• The tablet will dissolve rapidly on the tongue and can be swallowed with saliva. It is not necessary to take Zolmitriptan Disintegrating Tablets with liquid.
• If the headache returns, you can take another tablet after 2 hours. If the first dose does not relieve the migraine attack, do not take a second dose unless advised to do so by your health care provider. Do not take more than 10 mg in a 24-hour period.
• If your medicine has expired, throw it away.
• If you miss a dose of Zolmitriptan Disintegrating Tablets and you still have a headache, follow your doctor’s dosing instructions. Contact your doctor if you are unsure of what to do if you miss a dose. Do not use Zolmitriptan Disintegrating Tablets more often than prescribed. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Zolmitriptan Disintegrating Tablets.

Important safety information:

• Zolmitriptan Disintegrating Tablets may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Zolmitriptan Disintegrating Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Diabetes patients – Zolmitriptan Disintegrating Tablets may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.
• Additional monitoring of your dose or condition may be needed if you are taking oral contraceptives (birth control pills), cimetidine, or other migraine medicines.
• The long-term effects of repeated use of Zolmitriptan Disintegrating Tablets have not been studied. The safety for treating an average of more than 4 headaches in a 30 day period has not been established.
• Lab tests, including liver function, kidney function, lung function, blood pressure, fasting blood glucose, and blood cholesterol, may be performed while you use Zolmitriptan Disintegrating Tablets. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.
• Use Zolmitriptan Disintegrating Tablets with caution in the ELDERLY; they may be more sensitive to its effects.
• Zolmitriptan Disintegrating Tablets should not be used in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.
• If you are past menopause discuss the safety of using Zolmitriptan Disintegrating Tablets with your doctor or pharmacist.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zolmitriptan Disintegrating Tablets while you are pregnant. It is not known if Zolmitriptan Disintegrating Tablets are found in breast milk. If you are or will be breast-feeding while you use Zolmitriptan Disintegrating Tablets, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Zolmitriptan Disintegrating Tablets:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Abnormal skin sensations; dizziness; drowsiness; increased sensitivity to touch; nausea; pain; warm/cold sensations; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); heart attack; pounding in the chest; tightness, pain, pressure, or heaviness in jaw, neck, throat, and chest.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include severe drowsiness.

Proper storage of Zolmitriptan Disintegrating Tablets:

Store Zolmitriptan Disintegrating Tablets at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zolmitriptan Disintegrating Tablets out of the reach of children and away from pets.

General information:

• If you have any questions about Zolmitriptan Disintegrating Tablets, please talk with your doctor, pharmacist, or other health care provider.
• Zolmitriptan Disintegrating Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zolmitriptan Disintegrating Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Zolmitriptan (zohl-mi-TRIP-tan)
Brand Name: Zomig

Zolmitriptan Spray is used for:

Treating acute migraine headaches with or without aura (flashing lights, wavy lines, dark spots) in adults. It is not intended to prevent migraines.

Zolmitriptan Spray belongs to a group of medicines called “triptans.” It works by narrowing the widened vessels thought to cause migraine headaches.

Do NOT use Zolmitriptan Spray if:

• you are allergic to any ingredient in Zolmitriptan Spray
• you have a history of heart disease, uncontrolled high blood pressure, or are currently taking or have taken a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the past 14 days
• you have used an ergot alkaloid (eg, ergotamine) or other “triptan” migraine medicine in the last 24 hours
• you are currently taking sibutramine
• you have migraines caused by basal arteries or hemiplegia

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zolmitriptan Spray:

Some medical conditions may interact with Zolmitriptan Spray. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have heart disease (or a family history of heart disease), peripheral blood vessel disease, high cholesterol, high blood pressure, or diabetes
• if you have cluster headaches
• if you have factors that could lead to heart attacks (eg, overweight, smoking) or you are a postmenopausal woman

Some MEDICINES MAY INTERACT with Zolmitriptan Spray. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because they may decrease Zolmitriptan Spray’s effectiveness
• Sibutramine because the risk of side effects, such as serotonin syndrome (ie, restlessness, fever, excessive sweating, confusion, twitching, seizures, which can rarely be life-threatening), may be increased
• Other serotonin agonists (eg, sumatriptan) because they may increase the risk of Zolmitriptan Spray’s side effects
• Ergot alkaloids (eg, ergotamine) or MAO inhibitors (eg, phenelzine) because the risk of their side effects may be increased by Zolmitriptan Sprays

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zolmitriptan Spray may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zolmitriptan Spray:

Use Zolmitriptan Spray as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• An extra patient leaflet is available with Zolmitriptan Spray. Talk to your pharmacist if you have questions about this information.
• It is best to use Zolmitriptan Spray as soon as you notice the headache symptoms of a migraine attack.
• Additional benefit may be obtained if the patient lies down in a quiet, dark room after administering medication.
• Zolmitriptan Spray is intended for the relief of acute migraine attacks. It does not prevent or reduce the number of attacks. Use Zolmitriptan Spray only for acute migraine attacks.
• Avoid spraying Zolmitriptan Spray into the eyes.
• The protective cap must not be removed from Zolmitriptan Spray until you are ready to use it.
• Do NOT test the spray before use.
• Gently blow your nose, then sit down and tilt your head back slightly. Spray the prescribed dose into 1 nostril. If your headache returns, a second nasal spray may be used anytime after 2 hours of using the first dose. If you do not respond to the first nasal spray, do not use Zolmitriptan Spray a second time without first consulting your health care provider. Do not use more than a total of 10 mg of Zolmitriptan Spray in a 24-hour period.
• If your medicine has expired, throw it away.
• If you miss a dose of Zolmitriptan Spray and you still have a headache, follow your doctor’s dosing instructions. Contact your doctor if you are unsure of what to do if you miss a dose. Do not use Zolmitriptan Spray more often than prescribed. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Zolmitriptan Spray.

Important safety information:

• Zolmitriptan Spray may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Zolmitriptan Spray with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• The long-term effects of repeated use of this medication have not been studied. The safety for treating an average of more than 4 headaches in a 30-day period has not established.
• Diabetes patients – Zolmitriptan Spray may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.
• Additional monitoring of your dose or condition may be needed if you are taking oral contraceptives (birth control pills), cimetidine, or other migraine medicines.
• Lab tests, including liver function, kidney function, lung function, blood pressure, fasting blood glucose, and blood cholesterol, may be performed while you use Zolmitriptan Spray. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.
• Use Zolmitriptan Spray with caution in the ELDERLY; they may be more sensitive to its effects.
• Zolmitriptan Spray should not be used in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.
• If you are past menopause discuss the safety of using Zolmitriptan Spray with your doctor or pharmacist.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zolmitriptan Spray while you are pregnant. It is not known if Zolmitriptan Spray is found in breast milk. If you are or will be breast-feeding while you use Zolmitriptan Spray, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Zolmitriptan Spray:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Abnormal skin sensations; dizziness; drowsiness; increased sensitivity to touch; nausea; pain; warm/cold sensations; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); pounding in the chest; tightness, pain, pressure, or heaviness in jaw, neck, throat, and chest.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include severe drowsiness.

Proper storage of Zolmitriptan Spray:

Store Zolmitriptan Spray at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zolmitriptan Spray out of the reach of children and away from pets.

General information:

• If you have any questions about Zolmitriptan Spray, please talk with your doctor, pharmacist, or other health care provider.
• Zolmitriptan Spray is to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zolmitriptan Spray. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Zoledronic Acid (ZOE-le-DRON-ik AS-id)
Brand Name: Reclast

Zoledronic Acid is used for:

Treating osteoporosis (weak bones) in women who are past menopause. It is used to help build bone in men with osteoporosis and to reduce the risk of bone fractures due to osteoporosis in certain patients. It is used to treat and prevent osteoporosis in certain patients treated with corticosteroids (eg, prednisone). It may also be used to treat Paget disease or other conditions as determined by your doctor.

Zoledronic Acid is a bisphosphonate. It works by decreasing the breakdown of bone. This reduces the amount of calcium that is released into the blood from bones and helps to lower your blood calcium level.

Do NOT use Zoledronic Acid if:

• you are allergic to any ingredient in Zoledronic Acid or to any other bisphosphonate (eg, alendronate)
• you have severe kidney problems
• you have low calcium levels
• you are using another form of zoledronic acid

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zoledronic Acid:

Some medical conditions may interact with Zoledronic Acid. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have had asthma or other breathing problems from taking aspirin
• if you have a history of kidney problems, low blood calcium levels, blood clotting problems, anemia, or bone infection
• if you have a history of thyroid or parathyroid problems or if you have had thyroid or parathyroid surgery
• if you have poor nutrition, nutrient absorption problems (eg, “malabsorption syndrome”), have had sections of your intestines removed; or are unable to take calcium or vitamin D supplements
• if you have low blood volume, recent vomiting or diarrhea, decreased appetite, or if you are dehydrated
• if you have cancer or are receiving radiation or chemotherapy
• if you have dental problems or have planned dental surgery (eg, tooth extraction)

Some MEDICINES MAY INTERACT with Zoledronic Acid. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Aminoglycoside antibiotics (eg, gentamicin) or diuretics (eg, furosemide) because the risk of low blood calcium levels may be increased
• Corticosteroids (eg, prednisone) because the risk of jawbone problems may be increased
• Medicines that may harm the kidney (eg, amphotericin B, cyclosporine, nonsteroidal anti-inflammatory drugs [NSAIDs] [eg, ibuprofen], tacrolimus, vancomycin) or thalidomide because the risk of kidney problems may be increased. Ask your doctor if you are unsure if any of your medicines might harm the kidney

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zoledronic Acid may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zoledronic Acid:

Use Zoledronic Acid as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• An extra patient leaflet is available with Zoledronic Acid. Talk to your pharmacist if you have questions about this information.
• Zoledronic Acid is usually given as an injection at your doctor’s office, hospital, or clinic.
• Drink at least 2 full glasses (16 oz/480 mL) of fluid (eg, water) within a few hours before you receive Zoledronic Acid, as directed by your doctor.
• If you miss a dose of Zoledronic Acid, contact your doctor right away.

Ask your health care provider any questions you may have about how to use Zoledronic Acid.

Important safety information:

• Zoledronic Acid may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Zoledronic Acid with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Follow the diet and exercise program given to you by your health care provider. Talk to your doctor about taking a calcium and vitamin D supplement while you use Zoledronic Acid.
• You may develop flu-like symptoms, mild fever, muscle or joint aches, or headache after you receive Zoledronic Acid. If this occurs, a mild pain reliever (eg, acetaminophen, ibuprofen) may help to relieve these symptoms.
• Zoledronic Acid may cause jaw bone problems in some patients. Your risk may be greater if you have cancer, poor dental hygiene, or certain other conditions (eg, anemia, blood clotting problems, dental problems, infections). Your risk may also be greater if you use certain medicines or therapies (eg, chemotherapy, corticosteroids, radiation). Talk to your doctor about having a dental exam before you start to use Zoledronic Acid. Ask your doctor any questions you may have about dental treatment while you use Zoledronic Acid.
• Proper dental care is important while you are taking Zoledronic Acid. Brush and floss your teeth and visit the dentist regularly.
• Certain dental procedures should be avoided if possible while you are using Zoledronic Acid. Check with your doctor and dentist before having any dental treatments while using Zoledronic Acid.
• Lab tests, including kidney function, complete blood cell counts, and blood electrolyte levels (eg, calcium, magnesium, phosphate), may be performed while you use Zoledronic Acid. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.
• Use Zoledronic Acid with caution in the ELDERLY, especially those with kidney problems; they may be more sensitive its effects.
• Zoledronic Acid should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.
• PREGNANCY and BREAST-FEEDING: Do not use Zoledronic Acid if you are pregnant. It may cause harm to the fetus. Avoid becoming pregnant while you are taking it. If you think you may be pregnant, contact your doctor right away. It is not known if Zoledronic Acid is found in breast milk. Do not breast-feed while you are using Zoledronic Acid.

Possible side effects of Zoledronic Acid:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Diarrhea; dizziness; headache; mild bone, joint, or muscle pain; mild flu-like symptoms (eg, mild fever, muscle aches); mild itching, pain, or redness at the injection site; nausea; stomach pain or upset; tiredness; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); change in the amount of urine produced; eye pain, redness, or swelling; fever, chills, or persistent sore throat; irregular heartbeat; jaw pain or swelling; mental or mood changes (eg, depression); muscle cramps or spasms; numbness or tingling (especially around the mouth); severe bone, joint, or muscle pain; severe or persistent dizziness or headache; severe or persistent nausea, vomiting, or diarrhea; severe or persistent tiredness or weakness; shortness of breath; swelling of the hands, ankles, or feet.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include decreased urination; irregular heartbeat; mental or mood changes; muscle cramps; numbness or tingling (especially around the mouth).

Proper storage of Zoledronic Acid:

Zoledronic Acid is usually handled and stored by a health care provider. If you are using Zoledronic Acid at home, store Zoledronic Acid as directed by your pharmacist or health care provider. Keep Zoledronic Acid out of the reach of children and away from pets.

General information:

• If you have any questions about Zoledronic Acid, please talk with your doctor, pharmacist, or other health care provider.
• Zoledronic Acid is to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zoledronic Acid. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Ondansetron (on-DAN-se-tron)
Brand Name: Zofran ODT

Zofran ODT Orally Disintegrating Tablets are used for:

Preventing nausea and vomiting due to chemotherapy, radiation treatment, or surgery. It may also be used for other conditions as determined by your doctor.

Zofran ODT Orally Disintegrating Tablets are a serotonin 5-HT₃ receptor blocker. It works by blocking a chemical thought to be a cause of nausea and vomiting in certain situations (eg, chemotherapy).

Do NOT use Zofran ODT Orally Disintegrating Tablets if:

• you are allergic to any ingredient in Zofran ODT Orally Disintegrating Tablets

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zofran ODT Orally Disintegrating Tablets:

Some medical conditions may interact with Zofran ODT Orally Disintegrating Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have liver problems or phenylketonuria (PKU)

Some MEDICINES MAY INTERACT with Zofran ODT Orally Disintegrating Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Antineoplastic agents (eg, cyclophosphamide) because their effectiveness may be decreased by Zofran ODT Orally Disintegrating Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zofran ODT Orally Disintegrating Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zofran ODT Orally Disintegrating Tablets:

Use Zofran ODT Orally Disintegrating Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Take Zofran ODT Orally Disintegrating Tablets by mouth with or without food or water.
• Do not remove the tablet from the blister pack until you are ready to take Zofran ODT Orally Disintegrating Tablets. Make sure that your hands are dry when you open the blister pack. Do not push the tablet through the foil. Peel back the foil on the blister pack and place the tablet on your tongue. The tablet dissolves quickly and can be swallowed with saliva. Zofran ODT Orally Disintegrating Tablets may be taken with or without water. Take the tablet immediately after opening the blister pack. Do not store the removed tablet for future use.
• To prevent or reduce the possibility of nausea or vomiting, continue taking Zofran ODT Orally Disintegrating Tablets for the entire time recommended by your doctor even if you do not notice any nausea.
• If you miss a dose of Zofran ODT Orally Disintegrating Tablets, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Zofran ODT Orally Disintegrating Tablets.

Important safety information:

• Zofran ODT Orally Disintegrating Tablets may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Zofran ODT Orally Disintegrating Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Some of these products contain phenylalanine. If you must have a diet that is low in phenylalanine, ask your pharmacist if it is in your product.
• Zofran ODT Orally Disintegrating Tablets should be used with extreme caution in CHILDREN younger than 4 years old; safety and effectiveness in these children have not been confirmed.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zofran ODT Orally Disintegrating Tablets while you are pregnant. It is not known if Zofran ODT Orally Disintegrating Tablets are found in breast milk. If you are or will be breast-feeding while you use Zofran ODT Orally Disintegrating Tablets, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Zofran ODT Orally Disintegrating Tablets:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Constipation; diarrhea; dizziness; drowsiness; headache; tiredness; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; fever; skin tingling or numbness; trouble urinating; vision change or loss.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include fainting; severe dizziness; sudden, temporary blindness.

Proper storage of Zofran ODT Orally Disintegrating Tablets:

Store Zofran ODT Orally Disintegrating Tablets between 36 and 86 degrees F (2 and 30 degrees C) in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zofran ODT Orally Disintegrating Tablets out of the reach of children and away from pets.

General information:

• If you have any questions about Zofran ODT Orally Disintegrating Tablets, please talk with your doctor, pharmacist, or other health care provider.
• Zofran ODT Orally Disintegrating Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zofran ODT Orally Disintegrating Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Generic Name: Ondansetron (on-DAN-se-tron)
Brand Name: Zofran

Zofran Solution is used for:

Preventing nausea and vomiting associated with cancer chemotherapy, radiation treatment, or surgery. It may also be used for other conditions as determined by your doctor.

Zofran Solution is a serotonin 5-HT₃ receptor blocker. It works by blocking a chemical thought to be a cause of nausea and vomiting in certain situations (eg, chemotherapy).

Do NOT use Zofran Solution if:

• you are allergic to any ingredient in Zofran Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Zofran Solution:

Some medical conditions may interact with Zofran Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have liver problems

Some MEDICINES MAY INTERACT with Zofran Solution. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Antineoplastic agents (eg, cyclophosphamide) because their effectiveness may be decreased by Zofran Solution

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zofran Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Zofran Solution:

Use Zofran Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Take Zofran Solution by mouth with or without food.
• Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose.
• To prevent or reduce the possibility of nausea or vomiting, continue taking Zofran Solution for the entire time recommended by your doctor even if you do not notice any nausea.
• If you miss a dose of Zofran Solution, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Zofran Solution.

Important safety information:

• Zofran Solution may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Zofran Solution with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.
• Zofran Solution should be used with extreme caution in CHILDREN younger than 4 years old; safety and effectiveness in these children have not been confirmed.
• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zofran Solution while you are pregnant. It is not known if Zofran Solution is found in breast milk. If you are or will be breast-feeding while you use Zofran Solution, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Zofran Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Constipation; diarrhea; dizziness; drowsiness; headache; tiredness; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; fever; skin tingling or numbness; trouble urinating; vision change or loss.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org), or emergency room immediately. Symptoms may include fainting; severe dizziness; slowed/irregular heartbeat; sudden, temporary blindness.

Proper storage of Zofran Solution:

Store Zofran Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store the bottle upright. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zofran Solution out of the reach of children and away from pets.

General information:

• If you have any questions about Zofran Solution, please talk with your doctor, pharmacist, or other health care provider.
• Zofran Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people.
• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Zofran Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.