Archive for the ‘carbonic anhydrase inhibitors’ Category

Neptazane

Neptazane

Generic Name: methazolamide (meth a ZOLE a mide)

What is Neptazane (methazolamide)?

Methazolamide is a carbonic anhydrase inhibitor. Carbonic anhydrase is a protein in the body. Methazolamide reduces the activity of this protein.

Methazolamide is used to treat glaucoma. By inhibiting the actions of carbonic anhydrase, methazolamide reduces the amount of fluid produced in the eyes and therefore also reduces pressure.

Methazolamide may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Neptazane (methazolamide)?

Contact your doctor immediately if you experience a sore throat, fever, unusual bleeding or bruising, tingling or tremors in the hands or feet, pain in the side or groin, or a rash. These symptoms could be early signs of a serious side effect.

Use caution when driving, operating machinery, or performing other hazardous activities. Methazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Methazolamide may increase the sensitivity of the skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

What should I discuss with my healthcare provider before taking Neptazane (methazolamide)?

Tell your doctor if you have ever had an allergic reaction to a sulfa-based drug such as sulfamethoxazole (e.g., Bactrim, Septra, Gantanol). Methazolamide is also a sulfa-based drug, and you may have a similar reaction to it.

Before taking methazolamide, tell your doctor if you

are on aspirin therapy,

have liver disease,

have kidney disease,

have heart disease,

have lung disease, or

have a hormonal disease.

You may not be able to take methazolamide, or you may require a dosage adjustment special monitoring during treatment if you have any of the conditions listed above.

Methazolamide is in the FDA pregnancy category C. This means that it is not known whether methazolamide will be harm an unborn baby. Do not take methazolamide without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether methazolamide passes into breast . Do not take methazolamide without first talking to your doctor if you are breast-feeding a baby.

How should I take Neptazane (methazolamide)?

Take methazolamide exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Take each dose with a full glass of water. Take methazolamide with food if it causes stomach upset.

It is important to take methazolamide regularly to get the most benefit.

Store methazolamide at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical attention if an overdose is suspected.

Symptoms of a methazolamide overdose include drowsiness, decreased appetite, nausea, vomiting, dizziness, numbness or tingling, shaking, and ringing in the ears.

What should I avoid while taking Neptazane (methazolamide)?

Use caution when driving, operating machinery, or performing other hazardous activities. Methazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Methazolamide may increase the sensitivity of the skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

Neptazane (methazolamide) side effects

If you experience any of the following serious side effects, stop taking methazolamide and seek emergency medical attention or contact your doctor immediately:

an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

a sore throat or a fever;

unusual bleeding or bruising;

side or groin pain;

tingling or tremors in the hands or feet; or

a rash.

Other, less serious side effects may be more likely to occur. Continue to take methazolamide and talk to your doctor if you experience

decreased appetite, nausea, vomiting, constipation, diarrhea, or changes in taste;

drowsiness, dizziness, fatigue, or weakness;

nervousness or tremor;

headache or confusion;

increased sensitivity of the skin to sunlight;

worsening gout;

loss of blood sugar control (if you are diabetic);

ringing in your ears or hearing problems; or

changes in vision.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Neptazane (methazolamide)?

Before taking this medication, tell your doctor if you are taking any of the following medicines:

cyclosporine (Sandimmune);

primidone (Mysoline);

diflunisal (Dolobid;

aspirin, salsalate (Disalcid, Salflex, Salsitab, others), choline salicylate (Arthropan), magnesium salicylate (Doan’s, Magan, Mobidin), or other aspirin-like products (salicylates); or

lithium (Lithobid, Eskalith, others).

You may not be able to take methazolamide, or you may require a dosage adjustment or special monitoring during treatment.

Drugs other than those listed here may also interact with methazolamide. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including vitamins, minerals, and herbal products.

MZM

MZM

Generic Name: methazolamide (meth a ZOLE a mide)

What is MZM (methazolamide)?

Methazolamide is a carbonic anhydrase inhibitor. Carbonic anhydrase is a protein in the body. Methazolamide reduces the activity of this protein.

Methazolamide is used to treat glaucoma. By inhibiting the actions of carbonic anhydrase, methazolamide reduces the amount of fluid produced in the eyes and therefore also reduces pressure.

Methazolamide may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about MZM (methazolamide)?

Contact your doctor immediately if you experience a sore throat, fever, unusual bleeding or bruising, tingling or tremors in the hands or feet, pain in the side or groin, or a rash. These symptoms could be early signs of a serious side effect.

Use caution when driving, operating machinery, or performing other hazardous activities. Methazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Methazolamide may increase the sensitivity of the skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

What should I discuss with my healthcare provider before taking MZM (methazolamide)?

Tell your doctor if you have ever had an allergic reaction to a sulfa-based drug such as sulfamethoxazole (e.g., Bactrim, Septra, Gantanol). Methazolamide is also a sulfa-based drug, and you may have a similar reaction to it.

Before taking methazolamide, tell your doctor if you

are on aspirin therapy,

have liver disease,

have kidney disease,

have heart disease,

have lung disease, or

have a hormonal disease.

You may not be able to take methazolamide, or you may require a dosage adjustment special monitoring during treatment if you have any of the conditions listed above.

Methazolamide is in the FDA pregnancy category C. This means that it is not known whether methazolamide will be harm an unborn baby. Do not take methazolamide without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether methazolamide passes into breast . Do not take methazolamide without first talking to your doctor if you are breast-feeding a baby.

How should I take MZM (methazolamide)?

Take methazolamide exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Take each dose with a full glass of water. Take methazolamide with food if it causes stomach upset.

It is important to take methazolamide regularly to get the most benefit.

Store methazolamide at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical attention if an overdose is suspected.

Symptoms of a methazolamide overdose include drowsiness, decreased appetite, nausea, vomiting, dizziness, numbness or tingling, shaking, and ringing in the ears.

What should I avoid while taking MZM (methazolamide)?

Use caution when driving, operating machinery, or performing other hazardous activities. Methazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Methazolamide may increase the sensitivity of the skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

MZM (methazolamide) side effects

If you experience any of the following serious side effects, stop taking methazolamide and seek emergency medical attention or contact your doctor immediately:

an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

a sore throat or a fever;

unusual bleeding or bruising;

side or groin pain;

tingling or tremors in the hands or feet; or

a rash.

Other, less serious side effects may be more likely to occur. Continue to take methazolamide and talk to your doctor if you experience

decreased appetite, nausea, vomiting, constipation, diarrhea, or changes in taste;

drowsiness, dizziness, fatigue, or weakness;

nervousness or tremor;

headache or confusion;

increased sensitivity of the skin to sunlight;

worsening gout;

loss of blood sugar control (if you are diabetic);

ringing in your ears or hearing problems; or

changes in vision.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect MZM (methazolamide)?

Before taking this medication, tell your doctor if you are taking any of the following medicines:

cyclosporine (Sandimmune);

primidone (Mysoline);

diflunisal (Dolobid;

aspirin, salsalate (Disalcid, Salflex, Salsitab, others), choline salicylate (Arthropan), magnesium salicylate (Doan’s, Magan, Mobidin), or other aspirin-like products (salicylates); or

lithium (Lithobid, Eskalith, others).

You may not be able to take methazolamide, or you may require a dosage adjustment or special monitoring during treatment.

Drugs other than those listed here may also interact with methazolamide. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including vitamins, minerals, and herbal products.

Glauctabs

Glauctabs

Generic Name: methazolamide (meth a ZOLE a mide)

What is Glauctabs (methazolamide)?

Methazolamide is a carbonic anhydrase inhibitor. Carbonic anhydrase is a protein in the body. Methazolamide reduces the activity of this protein.

Methazolamide is used to treat glaucoma. By inhibiting the actions of carbonic anhydrase, methazolamide reduces the amount of fluid produced in the eyes and therefore also reduces pressure.

Methazolamide may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Glauctabs (methazolamide)?

Contact your doctor immediately if you experience a sore throat, fever, unusual bleeding or bruising, tingling or tremors in the hands or feet, pain in the side or groin, or a rash. These symptoms could be early signs of a serious side effect.

Use caution when driving, operating machinery, or performing other hazardous activities. Methazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Methazolamide may increase the sensitivity of the skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

What should I discuss with my healthcare provider before taking Glauctabs (methazolamide)?

Tell your doctor if you have ever had an allergic reaction to a sulfa-based drug such as sulfamethoxazole (e.g., Bactrim, Septra, Gantanol). Methazolamide is also a sulfa-based drug, and you may have a similar reaction to it.

Before taking methazolamide, tell your doctor if you

are on aspirin therapy,

have liver disease,

have kidney disease,

have heart disease,

have lung disease, or

have a hormonal disease.

You may not be able to take methazolamide, or you may require a dosage adjustment special monitoring during treatment if you have any of the conditions listed above.

Methazolamide is in the FDA pregnancy category C. This means that it is not known whether methazolamide will be harm an unborn baby. Do not take methazolamide without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether methazolamide passes into breast . Do not take methazolamide without first talking to your doctor if you are breast-feeding a baby.

How should I take Glauctabs (methazolamide)?

Take methazolamide exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Take each dose with a full glass of water. Take methazolamide with food if it causes stomach upset.

It is important to take methazolamide regularly to get the most benefit.

Store methazolamide at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical attention if an overdose is suspected.

Symptoms of a methazolamide overdose include drowsiness, decreased appetite, nausea, vomiting, dizziness, numbness or tingling, shaking, and ringing in the ears.

What should I avoid while taking Glauctabs (methazolamide)?

Use caution when driving, operating machinery, or performing other hazardous activities. Methazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Methazolamide may increase the sensitivity of the skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

Glauctabs (methazolamide) side effects

If you experience any of the following serious side effects, stop taking methazolamide and seek emergency medical attention or contact your doctor immediately:

an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

a sore throat or a fever;

unusual bleeding or bruising;

side or groin pain;

tingling or tremors in the hands or feet; or

a rash.

Other, less serious side effects may be more likely to occur. Continue to take methazolamide and talk to your doctor if you experience

decreased appetite, nausea, vomiting, constipation, diarrhea, or changes in taste;

drowsiness, dizziness, fatigue, or weakness;

nervousness or tremor;

headache or confusion;

increased sensitivity of the skin to sunlight;

worsening gout;

loss of blood sugar control (if you are diabetic);

ringing in your ears or hearing problems; or

changes in vision.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Glauctabs (methazolamide)?

Before taking this medication, tell your doctor if you are taking any of the following medicines:

cyclosporine (Sandimmune);

primidone (Mysoline);

diflunisal (Dolobid;

aspirin, salsalate (Disalcid, Salflex, Salsitab, others), choline salicylate (Arthropan), magnesium salicylate (Doan’s, Magan, Mobidin), or other aspirin-like products (salicylates); or

lithium (Lithobid, Eskalith, others).

You may not be able to take methazolamide, or you may require a dosage adjustment or special monitoring during treatment.

Drugs other than those listed here may also interact with methazolamide. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including vitamins, minerals, and herbal products.

Daranide

Daranide

Generic Name: dichlorphenamide (dye klor FEN a mide)

What is Daranide (dichlorphenamide)?

Dichlorphenamide is a carbonic anhydrase inhibitor. Carbonic anhydrase is a protein in your body. Dichlorphenamide reduces the activity of this protein.

Dichlorphenamide is used to treat glaucoma. By inhibiting the actions of carbonic anhydrase, dichlorphenamide reduces the amount of fluid produced in your eyes and therefore also reduces pressure.

Dichlorphenamide may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Daranide (dichlorphenamide)?

Call your doctor immediately if you experience a sore throat, fever, unusual bleeding or bruising, tingling or tremors in your hands or feet, pain in your side or groin, or a rash. These symptoms could be early signs of a serious side effect.

Use caution when driving, operating machinery, or performing other hazardous activities. Dichlorphenamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Dichlorphenamide may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

What should I discuss with my healthcare provider before taking Daranide (dichlorphenamide)?

Tell your doctor if you have ever had an allergic reaction to a sulfa-based drug such as sulfamethoxazole (e.g., Bactrim, Septra, Gantanol). Dichlorphenamide is also a sulfa-based drug, and you may have a similar reaction to it.

Before taking dichlorphenamide, tell your doctor if you

are on aspirin therapy,

have liver disease,

have kidney disease,

have heart disease,

have lung disease, or

have a hormonal disease.

You may not be able to take dichlorphenamide, or you may require a lower dose or special monitoring during treatment if you have any of the conditions listed above.

Dichlorphenamide is in the FDA pregnancy category C. This means that it is not known whether dichlorphenamide will harm an unborn baby. Do not take dichlorphenamide without first talking to your doctor if you are pregnant. It is not known whether dichlorphenamide passes into breast milk. Do not take dichlorphenamide without first talking to your doctor if you are breast-feeding a baby.

How should I take Daranide (dichlorphenamide)?

Take dichlorphenamide exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Take each dose with a full glass of water. Store dichlorphenamide at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and take only your next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical attention.

Symptoms of a dichlorphenamide overdose include drowsiness, decreased appetite, nausea, vomiting, dizziness, numbness or tingling, shaking, and ringing in the ears.

What should I avoid while taking Daranide (dichlorphenamide)?

Use caution when driving, operating machinery, or performing other hazardous activities. Dichlorphenamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Dichlorphenamide may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

Daranide (dichlorphenamide) side effects

If you experience any of the following serious side effects, seek emergency medical attention:

an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

a sore throat or a fever;

unusual bleeding or bruising;

side or groin pain;

tingling or tremors in your hands or feet; or

a rash.

Other, less serious side effects may be more likely to occur. Continue to take dichlorphenamide and talk to your doctor if you experience

decreased appetite, nausea, vomiting, constipation, diarrhea, or changes in taste;

drowsiness, dizziness, fatigue, or weakness;

nervousness or tremor;

headache or confusion;

increased sensitivity of the skin to sunlight;

worsening gout;

loss of blood sugar control (if you are diabetic);

ringing in your ears or hearing problems; or

changes in your vision.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

What other drugs will affect Daranide (dichlorphenamide)?

Before taking this medication, tell your doctor if you are taking any of the following medicines:

cyclosporine (Sandimmune). Cyclosporine may have more side effects if it is taken with dichlorphenamide.

primidone (Mysoline). Primidone may not be as effective if it is taken with dichlorphenamide, and seizure control may be reduced.

diflunisal (Dolobid). Diflunisal may increase both the activity and the side effects of dichlorphenamide.

aspirin, salsalate (Disalcid, Salflex, Salsitab, others), choline salicylate (Arthropan), magnesium salicylate (Doan’s, Magan, Mobidin), and other aspirin-like products (salicylates). These medicines may also interact with dichlorphenamide, and special monitoring of your therapy may be necessary.

lithium (Lithobid, Eskalith, others). Dichlorphenamide may decrease the level of lithium in your blood. Special monitoring or a dosage adjustment may be necessary.

Drugs other than those listed here may also interact with dichlorphenamide. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.

Diamox

Diamox

Generic Name: acetazolamide (a SEET a ZOLE a mide)

What is Diamox (acetazolamide)?

Acetazolamide is a carbonic anhydrase inhibitor. Carbonic anhydrase is a protein in your body. Acetazolamide reduces the activity of this protein.

Acetazolamide is used to treat glaucoma and to treat and to prevent acute mountain sickness (altitude sickness). It is also used as a part of some treatment plans for congestive heart failure and seizure disorders.

Acetazolamide may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Diamox (acetazolamide)?

Call your doctor immediately if you experience a sore throat, fever, unusual bleeding or bruising, tingling or tremors in your hands or feet, pain in your side or groin, or a rash. These symptoms could be early signs of a serious side effect.

Use caution when driving, operating machinery, or performing other hazardous activities. Acetazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Acetazolamide may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

Who should not take Diamox (acetazolamide)?

Tell your doctor if you have ever had an allergic reaction to a sulfa-based drug such as sulfamethoxazole (e.g., Bactrim, Septra, Gantanol). Acetazolamide is also a sulfa-based drug, and you may have a similar reaction to it.

Before taking acetazolamide, tell your doctor if you

are on aspirin therapy,

have liver disease,

have kidney disease,

have heart disease,

have lung disease, or

have a hormonal disease.

You may not be able to take acetazolamide, or you may require a lower dose or special monitoring during treatment if you have any of the conditions listed above.

Acetazolamide is in the FDA pregnancy category C. This means that it is not known whether acetazolamide will harm an unborn baby. Do not take acetazolamide without first talking to your doctor if you are pregnant. Acetazolamide passes into breast milk. It is not known whether acetazolamide will affect a nursing infant. Do not take acetazolamide without first talking to your doctor if you are breast-feeding a baby.

How should I take Diamox (acetazolamide)?

Take acetazolamide exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Take each dose with a full glass of water. Take acetazolamide with food if it upsets your stomach. Store acetazolamide at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and take only your next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical attention.

Symptoms of an acetazolamide overdose are not well known, but the following symptoms might be expected: drowsiness, decreased appetite, nausea, vomiting, dizziness, numbness or tingling, shaking, and ringing in the ears.

What should I avoid while taking Diamox (acetazolamide)?

Use caution when driving, operating machinery, or performing other hazardous activities. Acetazolamide may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Avoid prolonged exposure to sunlight. Acetazolamide may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

Diamox (acetazolamide) side effects

If you experience any of the following serious side effects, stop taking acetazolamide and seek emergency medical attention:

an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

a sore throat or a fever;

unusual bleeding or bruising;

side or groin pain;

tingling or tremors in your hands or feet; or

a rash.

Other, less serious side effects may be more likely to occur. Continue to take acetazolamide and talk to your doctor if you experience

decreased appetite, nausea, vomiting, constipation, diarrhea, or changes in taste;

drowsiness, dizziness, fatigue, or weakness;

nervousness or mild tremor;

headache or confusion;

increased sensitivity of the skin to sunlight;

worsening gout;

loss of blood sugar control (if you are diabetic);

ringing in your ears or hearing problems; or

changes in your vision.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Diamox (acetazolamide)?

Before taking this medication, tell your doctor if you are taking any of the following medicines:

cyclosporine (Sandimmune). Cyclosporine may have more side effects if it is taken with acetazolamide.

primidone (Mysoline). Primidone may not be as effective if it is taken with acetazolamide, and seizure control may be reduced.

diflunisal (Dolobid). Diflunisal may increase both the activity and the side effects of acetazolamide.

aspirin, salsalate (Disalcid, Salflex, Salsitab, others), choline salicylate (Arthropan), magnesium salicylate (Doan’s, Magan, Mobidin), and other aspirin-like products (salicylates). These medicines may also interact with acetazolamide, and special monitoring of your therapy may be necessary.

lithium (Lithobid, Eskalith, others). Acetazolamide may decrease the level of lithium in your blood. Special monitoring or a dosage adjustment may be necessary.

Drugs other than those listed here may also interact with acetazolamide. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.

Diamox Sequels

Diamox Sequels Sustained-Release Capsules

Diamox Sequels Sustained-Release Capsules are used for:

Treating certain types of glaucoma in combination with other medicines. It is also used to treat or prevent symptoms of mountain sickness. It may also be used for other conditions as determined by your doctor.

Diamox Sequels Sustained-Release Capsules are a carbonic anhydrase inhibitor. It reduces fluid pressure in the eyeball by decreasing fluid formation in the eyeball.

Do NOT use Diamox Sequels Sustained-Release Capsules if:

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

Before using Diamox Sequels Sustained-Release Capsules:

Some medical conditions may interact with Diamox Sequels Sustained-Release Capsules. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Diamox Sequels Sustained-Release Capsules. Tell your health care provider if you are taking any of the following medicines:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Diamox Sequels Sustained-Release Capsules 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 Diamox Sequels Sustained-Release Capsules:

Use Diamox Sequels Sustained-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Diamox Sequels Sustained-Release Capsules.

Important safety information:

Possible side effects of Diamox Sequels Sustained-Release Capsules:

All medicines may cause side effects, but many people have no, or minor, side effects.

Blurred vision; changes in taste; constipation; diarrhea; drowsiness; frequent urination; loss of appetite; nausea; vomiting.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blood in urine; changes in hearing; convulsions; dark, bloody stools; dark urine; fast breathing; fever; lack of energy; lower back pain; red, swollen, or blistered skin; ringing in the ears; sore throat; tingling of the arms or legs; unusual bleeding or bruising; vision changes; yellowing of the skin or eyes.

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

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Store Diamox Sequels Sustained-Release Capsules at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diamox Sequels Sustained-Release Capsules out of the reach of children and away from pets.

General information:

This information is summary only. It does not contain all information about Diamox Sequels Sustained-Release Capsules. 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.

More Diamox Sequels Sustained-Release Capsules resources

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