Archive for the ‘group I antiarrhythmics’ Category

Tonocard

Tonocard

Generic Name: tocainide (toe CANE ide)

What is Tonocard (tocainide)?

Tocainide affects the way that your heart beats.

Tocainide is used to treat serious irregularity in heartbeat patterns.

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

What is the most important information I should know about Tonocard (tocainide)?

Call your doctor immediately if you experience wheezing, coughing, difficulty breathing, chest pain, chest discomfort, worsening irregular heartbeats, a fever, a sore throat, a throat infection, a sore mouth, mouth ulcers, a rash, or unusual bruising or bleeding.

Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition much worse. Use caution when driving, operating machinery, or performing other hazardous activities. Tocainide may cause dizziness, drowsiness, or blurred vision. If you experience dizziness, drowsiness, or blurred vision, avoid these activities.

What should I discuss with my healthcare provider before taking Tonocard (tocainide)?

Before taking tocainide, tell your doctor if you have

any other type of heart disease or heart problem,

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

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

How should I take Tonocard (tocainide)?

Take tocainide 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. Tocainide may be taken with food to lessen stomach upset. Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition much worse. Store tocainide at room temperature away from moisture and heat.

What happens if I miss a dose?

Try not to miss any doses of this medication. Missing doses could be very dangerous.

If you do miss a dose, take it 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. A double dose could be dangerous.

What happens if I overdose?

Seek emergency medical attention.

Symptoms of a tocainide overdose include tiredness, dizziness, confusion, tremor, nausea, vomiting, seizures, and a worsening irregular heartbeat.

What should I avoid while taking Tonocard (tocainide)?

Use caution when driving, operating machinery, or performing other hazardous activities. Tocainide may cause dizziness, drowsiness, or blurred vision. If you experience dizziness, drowsiness, or blurred vision, avoid these activities.

Follow any other special instructions given by your doctor regarding food, beverages or activities.

Tonocard (tocainide) side effects

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

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

a new or a worsening irregular heartbeat pattern;

wheezing, coughing, chest pain, or chest discomfort;

unusual bruising or bleeding; or

fever, sore throat, a sore mouth, mouth ulcers, or an infection.

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

dizziness or tiredness;

upset stomach, vomiting, decreased appetite, or diarrhea;

headache or blurred vision;

confusion; or

numbness, tingling, or tremor (shaking).

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 Tonocard (tocainide)?

The effects of tocainide may be decreased by rifampin (Rimactane, Rifadin). Your doctor may want to adjust your tocainide dosage if you are taking this medicine.

The beta-blocker metoprolol (Lopressor) may increase the effects of tocainide. Your doctor may need to lower your dose of tocainide if you are taking this medication.

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

Quinidex Extentabs

Quinidex Extentabs

Generic Name: quinidine (KWIH nih deen)

What is Quinidex Extentabs (quinidine)?

Quinidine affects the way that the heart beats.

Quinidine is used to treat irregular heartbeat patterns.

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

What is the most important information I should know about Quinidex Extentabs (quinidine)?

Contact your doctor immediately if you experience ringing in the ears, changes in vision, dizziness, fainting, a rapid heartbeat, headache, nausea, a rash, or difficulty breathing.

Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition worse. Quinidine may be taken with food to lessen stomach upset. Do not crush, chew, or break any extended- or sustained-release formulations of quinidine. Swallow them whole. If you are not sure whether you have a long-acting form of quinidine, ask your pharmacist, nurse, or doctor.

What should I discuss with my healthcare provider before taking Quinidex Extentabs (quinidine)?

Before taking quinidine, tell your doctor if you have

had an allergic reaction or the development of blood problems (e.g., thrombocytopenic purpura) due to previous treatment with quinidine or quinine;

any other type of heart disease or heart problems;

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

Quinidine is in the FDA pregnancy category C. This means that it is not known whether quinidine will be harmful to an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant or could become pregnant during treatment. Quinidine passes into breast milk. It is not known whether quinidine will affect a nursing infant. Do not take this medication without first talking to your doctor if you are breast-feeding a baby.

How should I take Quinidex Extentabs (quinidine)?

Take quinidine 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. Quinidine may be taken with food to lessen stomach upset. Do not crush, chew, or break any extended- or sustained-release formulations of quinidine. Swallow them whole. If you are not sure whether you have a long-acting form of quinidine, ask your pharmacist, nurse, or doctor. Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition worse.

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

Your doctor may want you to have blood tests or other medical evaluations during treatment with quinidine to monitor progress and side effects.

Grapefruit and grapefruit juice may interact with quinidine. The interaction could lead to potentially adverse effects. You should discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Store quinidine 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. A double dose could be dangerous.

What happens if I overdose?

Seek emergency medical attention.

Symptoms of a quinidine overdose include confusion, tiredness, seizures, difficulty breathing, fainting, a rapid heartbeat, and coma.

What should I avoid while taking Quinidex Extentabs (quinidine)?

Grapefruit and grapefruit juice may interact with quinidine. The interaction could lead to potentially adverse effects. You should discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Quinidex Extentabs (quinidine) side effects

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

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

a new or a worsening irregular heartbeat pattern;

chest pain or chest discomfort;

ringing in the ears;

changes in vision;

dizziness, fainting, or headache;

rash;

difficulty breathing;

abdominal pain, nausea, or vomiting; or

yellowing of the skin or eyes.

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

mild upset stomach;

headache;

decreased appetite;

diarrhea; or

muscle weakness.

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 Quinidex Extentabs (quinidine)?

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

pimozide (Orap);

itraconazole (Sporanox);

ziprasidone (Geodon);

voriconazole (VFEND);

thioridazine (Mellaril) or mesoridazine (Serentil);

ritonavir (Norvir);

dolasetron (Anzemet);

digoxin (Lanoxin);

warfarin (Coumadin);

erythromycin (E-Mycin, Eryc, E.E.S., others);

sparfloxacin (Zagam), levofloxacin (Levaquin), grepafloxacin (Raxar), gatifloxacin (Tequin);

another medicine to treat irregular heartbeats such as bepridil (Vascor), dofetilide (Tikosyn), procainamide (Procan SR, Procanbid, Pronestyl), disopyramide (Norpace), and others;

a beta-blocker such as atenolol (Tenormin), metoprolol (Lopressor), propranolol (Inderal), and others;

a tricyclic antidepressant such as amitriptyline (Elavil), doxepin (Sinequan), clomipramine (Anafranil), imipramine (Tofranil), others; or

a phenothiazine such as chlorpromazine (Thorazine), promethazine (Phenergan, Promethegan), prochlorperazine (Compazine), and others.

You may not be able to take quinidine, or you may require a dosage adjustment or special monitoring if you are taking any of the medicines listed above.

Many drugs other than those listed here can interact with quinidine, resulting in dangerous side effects and/or decreased effectiveness. Do not take any other prescription or over-the-counter medications, including herbal products, during treatment with quinidine without first talking to your doctor or pharmacist.

Quinaglute Dura-Tabs

Quinaglute Dura-Tabs

Generic Name: quinidine (KWIH nih deen)

What is Quinaglute Dura-Tabs (quinidine)?

Quinidine affects the way that the heart beats.

Quinidine is used to treat irregular heartbeat patterns.

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

What is the most important information I should know about Quinaglute Dura-Tabs (quinidine)?

Contact your doctor immediately if you experience ringing in the ears, changes in vision, dizziness, fainting, a rapid heartbeat, headache, nausea, a rash, or difficulty breathing.

Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition worse. Quinidine may be taken with food to lessen stomach upset. Do not crush, chew, or break any extended- or sustained-release formulations of quinidine. Swallow them whole. If you are not sure whether you have a long-acting form of quinidine, ask your pharmacist, nurse, or doctor.

What should I discuss with my healthcare provider before taking Quinaglute Dura-Tabs (quinidine)?

Before taking quinidine, tell your doctor if you have

had an allergic reaction or the development of blood problems (e.g., thrombocytopenic purpura) due to previous treatment with quinidine or quinine;

any other type of heart disease or heart problems;

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

Quinidine is in the FDA pregnancy category C. This means that it is not known whether quinidine will be harmful to an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant or could become pregnant during treatment. Quinidine passes into breast milk. It is not known whether quinidine will affect a nursing infant. Do not take this medication without first talking to your doctor if you are breast-feeding a baby.

How should I take Quinaglute Dura-Tabs (quinidine)?

Take quinidine 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. Quinidine may be taken with food to lessen stomach upset. Do not crush, chew, or break any extended- or sustained-release formulations of quinidine. Swallow them whole. If you are not sure whether you have a long-acting form of quinidine, ask your pharmacist, nurse, or doctor. Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition worse.

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

Your doctor may want you to have blood tests or other medical evaluations during treatment with quinidine to monitor progress and side effects.

Grapefruit and grapefruit juice may interact with quinidine. The interaction could lead to potentially adverse effects. You should discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Store quinidine 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. A double dose could be dangerous.

What happens if I overdose?

Seek emergency medical attention.

Symptoms of a quinidine overdose include confusion, tiredness, seizures, difficulty breathing, fainting, a rapid heartbeat, and coma.

What should I avoid while taking Quinaglute Dura-Tabs (quinidine)?

Grapefruit and grapefruit juice may interact with quinidine. The interaction could lead to potentially adverse effects. You should discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Quinaglute Dura-Tabs (quinidine) side effects

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

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

a new or a worsening irregular heartbeat pattern;

chest pain or chest discomfort;

ringing in the ears;

changes in vision;

dizziness, fainting, or headache;

rash;

difficulty breathing;

abdominal pain, nausea, or vomiting; or

yellowing of the skin or eyes.

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

mild upset stomach;

headache;

decreased appetite;

diarrhea; or

muscle weakness.

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 Quinaglute Dura-Tabs (quinidine)?

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

pimozide (Orap);

itraconazole (Sporanox);

ziprasidone (Geodon);

voriconazole (VFEND);

thioridazine (Mellaril) or mesoridazine (Serentil);

ritonavir (Norvir);

dolasetron (Anzemet);

digoxin (Lanoxin);

warfarin (Coumadin);

erythromycin (E-Mycin, Eryc, E.E.S., others);

sparfloxacin (Zagam), levofloxacin (Levaquin), grepafloxacin (Raxar), gatifloxacin (Tequin);

another medicine to treat irregular heartbeats such as bepridil (Vascor), dofetilide (Tikosyn), procainamide (Procan SR, Procanbid, Pronestyl), disopyramide (Norpace), and others;

a beta-blocker such as atenolol (Tenormin), metoprolol (Lopressor), propranolol (Inderal), and others;

a tricyclic antidepressant such as amitriptyline (Elavil), doxepin (Sinequan), clomipramine (Anafranil), imipramine (Tofranil), others; or

a phenothiazine such as chlorpromazine (Thorazine), promethazine (Phenergan, Promethegan), prochlorperazine (Compazine), and others.

You may not be able to take quinidine, or you may require a dosage adjustment or special monitoring if you are taking any of the medicines listed above.

Many drugs other than those listed here can interact with quinidine, resulting in dangerous side effects and/or decreased effectiveness. Do not take any other prescription or over-the-counter medications, including herbal products, during treatment with quinidine without first talking to your doctor or pharmacist.

Quin-Release

Quin-Release

Generic Name: quinidine (KWIH nih deen)

What is Quin-Release (quinidine)?

Quinidine affects the way that the heart beats.

Quinidine is used to treat irregular heartbeat patterns.

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

What is the most important information I should know about Quin-Release (quinidine)?

Contact your doctor immediately if you experience ringing in the ears, changes in vision, dizziness, fainting, a rapid heartbeat, headache, nausea, a rash, or difficulty breathing.

Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition worse. Quinidine may be taken with food to lessen stomach upset. Do not crush, chew, or break any extended- or sustained-release formulations of quinidine. Swallow them whole. If you are not sure whether you have a long-acting form of quinidine, ask your pharmacist, nurse, or doctor.

What should I discuss with my healthcare provider before taking Quin-Release (quinidine)?

Before taking quinidine, tell your doctor if you have

had an allergic reaction or the development of blood problems (e.g., thrombocytopenic purpura) due to previous treatment with quinidine or quinine;

any other type of heart disease or heart problems;

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

Quinidine is in the FDA pregnancy category C. This means that it is not known whether quinidine will be harmful to an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant or could become pregnant during treatment. Quinidine passes into breast milk. It is not known whether quinidine will affect a nursing infant. Do not take this medication without first talking to your doctor if you are breast-feeding a baby.

How should I take Quin-Release (quinidine)?

Take quinidine 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. Quinidine may be taken with food to lessen stomach upset. Do not crush, chew, or break any extended- or sustained-release formulations of quinidine. Swallow them whole. If you are not sure whether you have a long-acting form of quinidine, ask your pharmacist, nurse, or doctor. Do not skip doses or change your dosing schedule without talking to your doctor. Changing your schedule could make your condition worse.

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

Your doctor may want you to have blood tests or other medical evaluations during treatment with quinidine to monitor progress and side effects.

Grapefruit and grapefruit juice may interact with quinidine. The interaction could lead to potentially adverse effects. You should discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Store quinidine 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. A double dose could be dangerous.

What happens if I overdose?

Seek emergency medical attention.

Symptoms of a quinidine overdose include confusion, tiredness, seizures, difficulty breathing, fainting, a rapid heartbeat, and coma.

What should I avoid while taking Quin-Release (quinidine)?

Grapefruit and grapefruit juice may interact with quinidine. The interaction could lead to potentially adverse effects. You should discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Quin-Release (quinidine) side effects

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

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

a new or a worsening irregular heartbeat pattern;

chest pain or chest discomfort;

ringing in the ears;

changes in vision;

dizziness, fainting, or headache;

rash;

difficulty breathing;

abdominal pain, nausea, or vomiting; or

yellowing of the skin or eyes.

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

mild upset stomach;

headache;

decreased appetite;

diarrhea; or

muscle weakness.

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 Quin-Release (quinidine)?

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

pimozide (Orap);

itraconazole (Sporanox);

ziprasidone (Geodon);

voriconazole (VFEND);

thioridazine (Mellaril) or mesoridazine (Serentil);

ritonavir (Norvir);

dolasetron (Anzemet);

digoxin (Lanoxin);

warfarin (Coumadin);

erythromycin (E-Mycin, Eryc, E.E.S., others);

sparfloxacin (Zagam), levofloxacin (Levaquin), grepafloxacin (Raxar), gatifloxacin (Tequin);

another medicine to treat irregular heartbeats such as bepridil (Vascor), dofetilide (Tikosyn), procainamide (Procan SR, Procanbid, Pronestyl), disopyramide (Norpace), and others;

a beta-blocker such as atenolol (Tenormin), metoprolol (Lopressor), propranolol (Inderal), and others;

a tricyclic antidepressant such as amitriptyline (Elavil), doxepin (Sinequan), clomipramine (Anafranil), imipramine (Tofranil), others; or

a phenothiazine such as chlorpromazine (Thorazine), promethazine (Phenergan, Promethegan), prochlorperazine (Compazine), and others.

You may not be able to take quinidine, or you may require a dosage adjustment or special monitoring if you are taking any of the medicines listed above.

Many drugs other than those listed here can interact with quinidine, resulting in dangerous side effects and/or decreased effectiveness. Do not take any other prescription or over-the-counter medications, including herbal products, during treatment with quinidine without first talking to your doctor or pharmacist.

Pronestyl-SR

Pronestyl-SR Controlled-Release

Taking Pronestyl-SR Controlled-Release for a prolonged period of time may lead to the development of antibodies in your blood that are sometimes associated with autoimmune diseases such as lupus. If you experience butterfly-shaped rash on the face, swollen or tender joints, unexplained fever, or severe or persistent tiredness, seizures, or mental or mood changes, contact your doctor.

Pronestyl-SR Controlled-Release should only be used to treat life-threatening irregular heartbeat. It has been associated with an increased risk of death when used to treat non-life-threatening irregular heartbeat. Talk with your doctor for more information.

Pronestyl-SR Controlled-Release may cause severe and sometimes fatal blood problems (eg, bone marrow suppression, low blood platelet or white blood cell levels, anemia). These side effects have occurred most often during the first 12 weeks of therapy. Lab tests, such as complete blood cell counts, may be performed weekly for the first 3 months of therapy and then periodically to monitor for these side effects. If you experience fever, chills, sore throat, mouth sores or irritation, or unusual bruising or bleeding, contact your doctor immediately. Your risk may be greater if you already have bone marrow or blood problems.

Pronestyl-SR Controlled-Release is used for:

Treating certain abnormal heart rhythms.

Pronestyl-SR Controlled-Release is an antiarrhythmic. It works by stabilizing the heart rhythm in conditions in which the heart is beating too fast or in an irregular rhythm (antiarrhythmic effect).

Do NOT use Pronestyl-SR Controlled-Release if:

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

Before using Pronestyl-SR Controlled-Release:

Some medical conditions may interact with Pronestyl-SR Controlled-Release. 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 Pronestyl-SR Controlled-Release. Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Pronestyl-SR Controlled-Release 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 Pronestyl-SR Controlled-Release:

Use Pronestyl-SR Controlled-Release 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 Pronestyl-SR Controlled-Release.

Important safety information:

Possible side effects of Pronestyl-SR Controlled-Release:

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

Bitter taste.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); butterfly-shaped rash on the face; chest pain; dark urine; depression; diarrhea; dizziness or lightheadedness; fainting; fast, slow, or irregular heartbeat; fever, chills, or sore throat; hallucinations; loss of appetite; mood or mental changes; mouth sores or irritation; muscle pain or weakness; nausea; pale stools; seizures; stomach pain; severe or persistent tiredness; shortness of breath; swollen or tender joints; unusual bruising or bleeding; unusual tiredness or weakness; vomiting; wheezing; 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 Pronestyl-SR Controlled-Release 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 Pronestyl-SR Controlled-Release out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Pronestyl-SR Controlled-Release. 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 Pronestyl-SR Controlled-Release resources

Compare Pronestyl-SR Controlled-Release with other medications for the treatment of:

Pronestyl

Pronestyl

Taking Pronestyl for a prolonged period of time may lead to the development of antibodies in your blood that are sometimes associated with autoimmune diseases such as lupus. If you experience butterfly-shaped rash on the face, swollen or tender joints, unexplained fever, or severe or persistent tiredness, seizures, or mental or mood changes, contact your doctor.

Pronestyl should only be used to treat life-threatening irregular heartbeat. It has been associated with an increased risk of death when used to treat non-life-threatening irregular heartbeat. Talk with your doctor for more information.

Pronestyl may cause severe and sometimes fatal blood problems (eg, bone marrow suppression, low blood platelet or white blood cell levels, anemia). These side effects have occurred most often during the first 12 weeks of therapy. Lab tests, such as complete blood cell counts, may be performed weekly for the first 3 months of therapy and then periodically to monitor for these side effects. If you experience fever, chills, sore throat, mouth sores or irritation, or unusual bruising or bleeding, contact your doctor immediately. Your risk may be greater if you already have bone marrow or blood problems.

Pronestyl is used for:

Treating certain abnormal heart rhythms.

Pronestyl is an antiarrhythmic. It works by stabilizing the heart rhythm in conditions in which the heart is beating too fast or in an irregular rhythm (antiarrhythmic effect).

Do NOT use Pronestyl if:

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

Before using Pronestyl :

Some medical conditions may interact with Pronestyl . 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 Pronestyl . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Pronestyl 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 Pronestyl :

Use Pronestyl 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 Pronestyl .

Important safety information:

Possible side effects of Pronestyl :

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

Bitter taste.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); butterfly-shaped rash on the face; chest pain; dark urine; depression; diarrhea; dizziness or lightheadedness; fainting; fast, slow, or irregular heartbeat; fever, chills, or sore throat; hallucinations; loss of appetite; mood or mental changes; mouth sores or irritation; muscle pain or weakness; nausea; pale stools; seizures; stomach pain; severe or persistent tiredness; shortness of breath; swollen or tender joints; unusual bruising or bleeding; unusual tiredness or weakness; vomiting; wheezing; 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 Pronestyl 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 Pronestyl out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Pronestyl . 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 Pronestyl resources

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Procanbid

Procanbid Controlled-Release

Taking Procanbid Controlled-Release for a prolonged period of time may lead to the development of antibodies in your blood that are sometimes associated with autoimmune diseases such as lupus. If you experience butterfly-shaped rash on the face, swollen or tender joints, unexplained fever, or severe or persistent tiredness, seizures, or mental or mood changes, contact your doctor.

Procanbid Controlled-Release should only be used to treat life-threatening irregular heartbeat. It has been associated with an increased risk of death when used to treat non-life-threatening irregular heartbeat. Talk with your doctor for more information.

Procanbid Controlled-Release may cause severe and sometimes fatal blood problems (eg, bone marrow suppression, low blood platelet or white blood cell levels, anemia). These side effects have occurred most often during the first 12 weeks of therapy. Lab tests, such as complete blood cell counts, may be performed weekly for the first 3 months of therapy and then periodically to monitor for these side effects. If you experience fever, chills, sore throat, mouth sores or irritation, or unusual bruising or bleeding, contact your doctor immediately. Your risk may be greater if you already have bone marrow or blood problems.

Procanbid Controlled-Release is used for:

Treating certain abnormal heart rhythms.

Procanbid Controlled-Release is an antiarrhythmic. It works by stabilizing the heart rhythm in conditions in which the heart is beating too fast or in an irregular rhythm (antiarrhythmic effect).

Do NOT use Procanbid Controlled-Release if:

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

Before using Procanbid Controlled-Release:

Some medical conditions may interact with Procanbid Controlled-Release. 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 Procanbid Controlled-Release. Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Procanbid Controlled-Release 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 Procanbid Controlled-Release:

Use Procanbid Controlled-Release 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 Procanbid Controlled-Release.

Important safety information:

Possible side effects of Procanbid Controlled-Release:

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

Bitter taste.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); butterfly-shaped rash on the face; chest pain; dark urine; depression; diarrhea; dizziness or lightheadedness; fainting; fast, slow, or irregular heartbeat; fever, chills, or sore throat; hallucinations; loss of appetite; mood or mental changes; mouth sores or irritation; muscle pain or weakness; nausea; pale stools; seizures; stomach pain; severe or persistent tiredness; shortness of breath; swollen or tender joints; unusual bruising or bleeding; unusual tiredness or weakness; vomiting; wheezing; 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 Procanbid Controlled-Release 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 Procanbid Controlled-Release out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Procanbid Controlled-Release. 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.

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Procan SR

Procan SR

Generic Name: procainamide (injection) (proe KANE a mide)

What is Procan SR (procainamide (injection))?

Procainamide affects the way your heart beats.

Procainamide is used to help keep the heart beating normally in people with certain heart rhythm disorders of the ventricles (the lower chambers of the heart that allow blood to flow out of the heart).

Procainamide may be used for other purposes not listed in this medication guide.

What is the most important information I should know about Procan SR (procainamide (injection))?

Procainamide is given in a hospital setting. Your heart rate, breathing, blood pressure and other vital signs will be watched closely while you are receiving procainamide. You should not use this medication if you are allergic to procainamide, or if you have certain heart conditions, especially “AV block” (unless you have a pacemaker), lupus, or a history of “Long QT syndrome.” If possible, before you receive procainamide, tell your doctor if you have congestive heart failure, circulation problems, a history of heart attack or stroke (including “mini-stroke”), a weak immune system, kidney or liver disease, myasthenia gravis, asthma, or if you are allergic to aspirin, sulfites, or any type of numbing medicine.

In an emergency situation, it may not be possible before you are treated to tell your caregivers about any health conditions you have or if you are pregnant or breast-feeding. However, make sure any doctor caring for you afterward knows that you have received this medication.

Procainamide can lower blood cells that help your body fight infections. Tell your doctor if you develop signs of infection such as fever, chills, sore throat, flu symptoms, easy bruising or bleeding (nosebleeds, bleeding gums), loss of appetite, nausea and vomiting, mouth sores, or unusual weakness.

What should I discuss with my healthcare provider before receiving Procan SR (procainamide (injection))?

You should not receive this medication if you are allergic to procainamide, or if you have:

certain heart conditions, especially “AV block” (unless you have a pacemaker);

lupus; or

a history of “Long QT syndrome.”

If you any of these other conditions, you may need a dose adjustment or special tests to safely use this medication:

congestive heart failure;

circulation problems;

a history of heart attack or stroke (including “mini-stroke”);

a weak immune system;

myasthenia gravis;

asthma or sulfite allergy;

if you are allergic to aspirin; or

if you have ever had an allergic reaction to a numbing medicine.

In an emergency situation, it may not be possible before you are treated with procainamide to tell your caregivers if you are pregnant or breast-feeding. However, make sure any doctor caring for your pregnancy or your baby knows that you have received this medication.

How is procainamide injection given?

Procainamide is given as an injection through a needle placed into a vein or muscle. You will receive procainamide injection in a hospital setting where your heart can be monitored in case the medication causes serious side effects.

Your heart rate will be constantly monitored using an electrocardiograph or ECG (sometimes called an EKG). This machine measures electrical activity of the heart. Your breathing, blood pressure and other vital signs will be watched closely while you are receiving procainamide.

Procainamide can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. Contact your doctor at once if you develop signs of infection such as fever, chills, sore throat, flu symptoms, easy bruising or bleeding (nosebleeds, bleeding gums), loss of appetite, nausea and vomiting, mouth sores, or unusual weakness.

To be sure this medication is not causing harmful effects, your blood may need to be tested on a regular basis. Do not miss any follow-up visits to your doctor.

What happens if I miss a dose?

Since procainamide injection is given as needed by a healthcare professional, it is not likely that you will miss a dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include drowsiness, tremors, weak or shallow breathing, and fainting.

What should I avoid while receiving Procan SR (procainamide (injection))?

Avoid being near people who have colds, the flu, or other contagious illnesses. Contact your doctor at once if you develop signs of infection.

Procainamide can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.

Procan SR (procainamide (injection)) side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

a new or a worsening irregular heartbeat pattern;

chest pain, wheezing, trouble breathing;

feeling like you might pass out;

signs of infection such as fever, chills, sore throat, flu symptoms, easy bruising or bleeding (nosebleeds, bleeding gums), loss of appetite, nausea and vomiting, mouth sores, unusual weakness;

depressed mood, hallucinations, severe dizziness;

stomach pain, nausea, vomiting, loss of appetite, dark urine, jaundice (yellowing of the skin or eyes); or

joint pain or swelling with fever, swollen glands, muscle pain or weakness, unusual thoughts or behavior, patchy skin color, red spots.

Less serious side effects may include:

mild dizziness or tired feeling;

upset stomach, diarrhea; or

mild itching.

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 Procan SR (procainamide (injection))?

Tell your doctor about all other medicines you use, especially:

cimetidine (Tagamet, Tagamet HB);

digoxin (digitalis, Lanoxin); or

heart rhythm medications such as amiodarone (Cordarone), quinidine (Quinaglute, Quinidex, Quin-Release), disopyramide (Norpace), flecaininde (Tambocor), mexiletine (Mexitil), morizicine (Ethmozine), propafenone, (Rythmol), and others.

This list is not complete and there may be other drugs that can interact with procainamide injection. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.

Where can I find more information?

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Norpace CR

Norpace CR Sustained-Release Capsules

Norpace CR Sustained-Release Capsules sometimes produces new irregular heartbeats (arrhythmias). Therefore, it should be used in carefully selected patients. Consult your doctor or pharmacist for more information.

Norpace CR Sustained-Release Capsules are used for:

Correcting or preventing various types of life-threatening irregular heartbeats and heart rhythm disturbances.

Norpace CR Sustained-Release Capsules are an antiarrhythmic. It works by stabilizing the heart rhythm in conditions in which the heart is beating too fast or in an irregular rhythm (antiarrhythmic effect).

Do NOT use Norpace CR Sustained-Release Capsules if:

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

Before using Norpace CR Sustained-Release Capsules:

Some medical conditions may interact with Norpace CR 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 Norpace CR Sustained-Release Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:

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

Use Norpace CR 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 Norpace CR Sustained-Release Capsules.

Important safety information:

Possible side effects of Norpace CR Sustained-Release Capsules:

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

Aches or pain; bloating; blurred vision; constipation; difficulty urinating; dizziness; dryness of the eyes, mouth, nose, or throat; fatigue; frequent and urgent urination; gas; general body discomfort; headache; muscle weakness; nausea; tiredness.

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; fainting; fast or slow heartbeat; fever; lightheadedness; heart rhythm problems; severe difficulty urinating; shortness of breath; sore throat; swelling.

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 Norpace CR Sustained-Release Capsules 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. Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Keep Norpace CR Sustained-Release Capsules out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Norpace CR 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 Norpace CR Sustained-Release Capsules resources

Mexitil

Mexitil

Because Mexitil may cause an irregular heartbeat in some patients, it should only be used to treat life-threatening irregular heartbeat.

Mexitil is used for:

Treating certain types of life-threatening irregular heartbeat.

Mexitil is an antiarrhythmic. It works by stabilizing the heart rhythm, which helps keep the heart from beating too fast or in an irregular rhythm.

Do NOT use Mexitil if:

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

Before using Mexitil :

Some medical conditions may interact with Mexitil . 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 Mexitil . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Mexitil 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 Mexitil :

Use Mexitil 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 Mexitil .

Important safety information:

Possible side effects of Mexitil :

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

Blurred vision; clumsiness; constipation; diarrhea; dizziness or lightheadedness; headache; heartburn; incoordination; nausea; nervousness; stomach discomfort; tremor; vomiting.

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision or other vision problems; chest pain; fainting; fever; irregular, fast, or slow heartbeat; severe dizziness or lightheadedness; severe stomach pain; sore throat; 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 Mexitil below 86 degrees F (30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Mexitil out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Mexitil . 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 Mexitil resources

Compare Mexitil with other medications for the treatment of:

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