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Monthly Archives: June 2010
Azathioprine sodium injection
Azathioprine sodium injection
Drug Name Azathioprine sodium injection
Azathioprine sodium injection Drug Category AZATHIOPRINE – INJECTION
Azathioprine sodium injection Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. AZATHIOPRINE – INJECTION (aze-uh-THIGH-oh-preen) COMMON BRAND NAME(S): Imuran WARNING: Long-term use of this medication increases the risk of developing neoplasias (cancerous or noncancerous growths). Azathioprine can also cause blood disorders (e.g., leukopenia). Immediately notify your doctor if you develop unusual growths, easy bruising or bleeding, or signs of infection such as persistent sore throat or fever. USES: This medication alters the body’s immune system so that your body does not reject a transplanted organ. It is also used to treat severe rheumatoid arthritis after other treatments have failed to provide relief. HOW TO USE: This drug may be given by vein (IV) until you are able to take the tablet form by mouth. It is usually given once daily. Dosage is adjusted based on your condition and response. Follow all instructions for proper mixing and dilution with certain IV fluids. Consult your pharmacist. This drug product should be checked visually for particles or discoloration before use. If present, do not use the liquid. SIDE EFFECTS: Nausea/vomiting, loss of appetite, diarrhea or pain at the injection site may occur. If these effects persist or worsen, notify your doctor promptly. Unlikely but report promptly: hair loss, unusual fatigue, stomach pain, joint or muscle pain, vision changes. Very unlikely but report promptly: yellowing of eyes or skin, darkened urine, unusual bleeding or bruising, lumps/growths. In the unlikely event you have an allergic reaction to this drug, seek immediate medical attention. Symptoms of an allergic reaction include: rash, itching, swelling, dizziness, trouble breathing. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Tell your doctor your medical history, including: allergies, liver or kidney disease, blood disorders, infections. This medication can lower the body’s ability to fight an infection. Notify your doctor promptly if you develop signs of an infection such as fever, chills or persistent sore throat. This drug is not recommended for use during pregnancy. Consult your doctor before using this drug. This drug is excreted into breast milk. Because of the potential risk to the infant, breast-feeding while using this drug is not recommended. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Tell your doctor of all nonprescription and prescription medication you use, especially of: allopurinol, drugs affecting bone marrow (e.g., cotrimoxazole, numerous anti-cancer drugs), “alkylating” type cancer drugs (e.g., melphalan, cyclophosphamide, chlorambucil), other immune suppressants (e.g., cyclosporine), “blood thinners” (e.g., warfarin, heparin), ACE inhibitors (e.g., captopril, lisinopril). Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. Symptoms of overdose may include nausea, vomiting, and diarrhea. NOTES: Do not share this medication with others. Laboratory and/or medical tests may be performed to monitor for side effects or response to treatment. MISSED DOSE: If the dose is missed, contact your doctor immediately to establish a new dosing schedule. STORAGE: Store at room temperature between 59 and 77 degrees F (15 – 25 degrees C) away from light and moisture. After mixing and dilution in IV fluids (consult your pharmacist for details), this product is stable at room temperature for 24 hours. Discard any unused portion of the vial. MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854-1166 (USA), or 1-800-668-1507 (Canada).
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Tagged Azathioprine, Azathioprine sodium, drug, information, injection, medication
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Azathioprine oral
Azathioprine oral
Drug Name Azathioprine oral
Azathioprine oral Drug Category AZATHIOPRINE – ORAL
Azathioprine oral Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. AZATHIOPRINE – ORAL (aze-uh-THIGH-oh-preen) COMMON BRAND NAME(S): Imuran WARNING: Long-term use of this medication increases the risk of developing neoplasias (cancerous or noncancerous growths). Azathioprine can also cause blood disorders (e.g., leukopenia). Immediately notify your doctor if you develop unusual growths, easy bruising or bleeding, or signs of infection such as persistent sore throat or fever. USES: Azathioprine is used to prevent rejection of transplanted organs and for cases of severe arthritis that do not respond to other therapies. OTHER USES: This medication may also be used to treat ulcerative colitis and for other purposes as determined by your doctor. HOW TO USE: Azathioprine tablets should be taken with food or milk to prevent stomach upset. Take this medication exactly as prescribed. Do not stop taking the medication without your doctor’s approval. SIDE EFFECTS: Nausea/vomiting, loss of appetite or diarrhea may occur. If these effects persist or worsen, notify your doctor promptly. Unlikely but report promptly: hair loss, unusual fatigue, stomach pain, joint or muscle pain, vision changes. Very unlikely but report promptly: yellowing of eyes or skin, darkened urine, unusual bleeding or bruising, unusual lumps or growths. In the unlikely event you have an allergic reaction to this drug, seek medical attention immediately. Symptoms of an allergic reaction include: rash, itching, swelling, dizziness, trouble breathing. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Before you take azathioprine, tell your doctor your medical history especially if you have: liver disease, kidney disease, blood disorders, any infection, any allergies. This medication can increase your risk of developing an infection. Notify your doctor at the first sign of a possible infection (fever, persistent sore throat). Azathioprine is not recommended for use during pregnancy. Consult your doctor before using it. This drug is excreted into breast milk. Breast-feeding while using this medication is not recommended. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Tell your doctor of all drugs you may use, (both prescription and nonprescription), especially of: blood thinners (e.g., warfarin, heparins), allopurinol, drugs affecting bone marrow (e.g., cotrimoxazole, numerous anti-cancer drugs), “alkylating” type cancer drugs (e.g., chlorambucil, melphalan, cyclosporine), ACE inhibitors (e.g., lisinopril). Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. Symptoms of overdose may include nausea, vomiting, and diarrhea. NOTES: Lab tests will be done frequently while taking this medication to monitor its effects. Do not allow anyone else to take this medication. MISSED DOSE: If you take this once daily and miss a dose, take it as soon as remembered but not if it is almost time for the next dose. Skip the missed dose and resume regular schedule. Do not double-up the dose to catch up. If you take this several times daily and miss one dose, take it as soon as you can or double-up the very next dose. If you miss more than one dose, contact your doctor. You may need to have your dosing schedule adjusted. STORAGE: Store at room temperature away from moisture and sunlight. Do not store in the bathroom. MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854-1166 (USA), or 1-800-668-1507 (Canada).
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Tagged Azathioprine, drug, information, medication, oral
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Azatadine maleate oral
Azatadine maleate oral
Drug Name Azatadine maleate oral
Azatadine maleate oral Drug Category ANTIHISTAMINES – ORAL
Azatadine maleate oral Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. ANTIHISTAMINES – ORAL USES: Antihistamines are used to treat rash, hives, watery eyes, runny nose, itching, and sneezing due to allergies or the common cold. They may also be used to treat motion sickness, anxiety, or as a sleep aid (for insomnia). HOW TO USE: May be taken with food or milk if stomach upset occurs. Sustained-release or long acting tablets and capsules must be swallowed whole. Chewing or crushing them will destroy the long action and may increase side effects. For chewable tablets, chew thoroughly and swallow. Shake suspensions well before taking. SIDE EFFECTS: May cause drowsiness, dizziness, headache, loss of appetite, stomach upset, vision changes, irritability, dry mouth and nose. These effects should subside as your body adjusts to the medication. If they persist or become bothersome, inform your doctor. Notify your doctor if you develop: breathing difficulties, pounding or irregular heartbeat, ringing in the ears, difficulty urinating. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Tell your doctor your medical history, especially of: glaucoma (narrow angle), stomach ulcers, difficulty urinating (e.g., enlarged prostate), heart disease, high blood pressure, seizures, lung problems, overactive thyroid. Change from a seated or lying position slowly to avoid dizziness. Use caution in performing activities requiring alertness. Limit alcohol intake to avoid excessive drowsiness. Caution is advised when using this drug in the elderly because they may be more sensitive to the effects of the drug. Do not give long-acting antihistamines to a child younger than 12 years of age nor other dose forms of antihistamines to a child younger than 6 years of age without doctor approval. This drug should be used only when clearly needed during pregnancy. Discuss the risks and benefits with your doctor. This medication may be excreted into breast milk. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Tell your doctor of all the medications you may use (both prescription and nonprescription), especially of: sleeping pills, sedatives, tranquilizers, muscle relaxants, medication for depression, seizure medications, narcotic pain relievers, other medications for colds/hay fever/allergies. Because this medication may affect allergy testing, you may have to stop using this medication for several days before the tests are performed. Consult your doctor about this. Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. Symptoms of overdose in children may include abnormal eye movements, flushed face, dry mouth, change in amount of urine, fever, excitation, agitation, bizarre behavior, confusion, restlessness, irritability, delirium, twitching, tiredness, abnormal tongue movement, trembling extremities, slurred speech, or seizures. Symptoms of overdose in adults may include drowsiness, or unconsciousness, which may be followed by excitement or seizures. NOTES: Do not share this product with others. MISSED DOSE: If you miss a dose, take as soon as remembered; do not take if it is almost time for the next dose, instead, skip the missed dose and resume your usual dosing schedule. Do not “double-up” the dose to catch up. STORAGE: Store at room temperature between 59 and 86 degrees F (between 15 and 30 degrees C) away from moisture and sunlight. Do not store in the bathroom. Do not freeze liquid forms of this medication. MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854-1166 (USA), or 1-800-668-1507 (Canada).
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Tagged Azatadine, Azatadine maleate, drug, information, medication, oral
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Avobenzone and Octocrylene topical
Avobenzone and Octocrylene topical
Drug Name Avobenzone and Octocrylene topical
Avobenzone and Octocrylene topical Drug Category SUNSCREENS
Avobenzone and Octocrylene topical Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. SUNSCREENS USES: Sunscreens are used to protect the skin from the sun preventing sunburn, premature aging, skin reactions and reducing the risk of skin cancer. HOW TO USE: Sunscreens are for topical use only. Apply liberally to all exposed skin 30 minutes before sun exposure. Reapply after swimming or excessive sweating. Wear protective eye covering. Use carefully when applying to the face. Avoid contact with the eyes. Use cautiously or avoid use on irritated skin. Do not use on infants under 6 months old. Children under 3 years should use a sunscreen with SPF of 30. SIDE EFFECTS: If a sunscreen causes redness or a rash, discontinue use. Talk to your doctor or pharmacist about using a different type of sunscreen product. Some sunscreen products may stain clothing. Apply with caution. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: If you have any of the following health problems, consult your doctor before using this medication: PABA allergy, benzocaine allergy, sulfa drug allergy. DRUG INTERACTIONS: Tell your doctor of any over-the-counter or prescription medication you may take including: skin products, sulfa-drugs, tetracycline, all antibiotics. Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. This medicine may be harmful if swallowed. NOTES: There are various types of sunscreens available in cream, lotion, gel, stick and spray form. The sun produces two types of ultraviolet radiation (UV); UVA and UVB. UVA radiation causes skin damage and skin reactions to medications, soaps, cosmetics and other chemicals. UVB radiation is responsible for sunburns and skin cancer. Sun Protection Factor (SPF) is a rating that indicates the degree of protection from the sun a product provides. The higher the number, the greater the protection. An SPF of at least 15 is recommended. SPF 30 is the upper limit, meaning that numbers greater than 30 provide no greater benefit. Waterproof products provide protection after being in the water for up to 80 minutes. Water-resistant products protect for up to 40 minutes and sweat-resistant products protect for up to 30 minutes of heavy sweating. Remember too that water, sand and snow reflect the sun. MISSED DOSE: Apply sunscreens liberally and often when outdoors. STORAGE: Store at room temperature between 59 and 86 degrees F (15 to 30 degrees C) away from heat and light. It is recommended to replace sunscreen products every year as they lose potency over time.
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Tagged Avobenzone, drug, information, medication, Octocrylene, topical
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Aurothioglucose intramusc
Aurothioglucose intramusc.
Drug Name Aurothioglucose intramusc.
Aurothioglucose intramusc. Drug Category AUROTHIOGLUCOSE – INJECTION
Aurothioglucose intramusc. Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. AUROTHIOGLUCOSE – INJECTION (are-oh-thigh-oh-GLUE-kose) COMMON BRAND NAME(S): Solganal WARNING: This medication can cause severe, even fatal, side effects including blood cell problems (decreased white blood cells and platelets). Immediately notify your doctor if you have signs of an infection (such as persistent sore throat or fever), unusual fatigue, dark or pink-reddish urine, itching, rash, mouth sores or irritation (stomatitis), or persistent diarrhea. Your doctor will be closely monitoring certain lab tests (e.g., white blood cells, platelets) before starting therapy and before you receive each injected dose or written prescription. USES: This medication is used to treat arthritis (rheumatoid) along with other medications. Also, this medication is usually used in combination with rest and physical therapy for arthritis. OTHER USES: This drug may also be used for other forms of arthritis. HOW TO USE: Shake this suspension well before using. This drug is given by injection into a muscle (IM), generally once a week initially. As treatment continues, the drug is generally given every 3-4 weeks. This should not be given by vein (IV). To minimize side effects, it is advised to be lying down when receiving this drug, and for ten minutes afterward. Beneficial effects occur slowly and 6 to 8 weeks treatment may be required before improvement occurs. Treatment is continued indefinitely, depending on any side effects and/or improvement in your condition. SIDE EFFECTS: Temporary joint pain may occur. Also, for short periods after injections, flushing, dizziness, sweating, headache or blurred vision may occur. If these persist or worsen, notify your doctor promptly. Report promptly: itching, skin redness or rash, sore mouth, stomach upset, metallic taste, persistent diarrhea, skin color change, vaginal discomfort. Very unlikely but report promptly: unusual bleeding or bruising, pink-reddish urine, fever or persistent sore throat, unusual fatigue, yellowing eyes or skin, abdominal pain, vision changes, confusion, seizures, hair loss. In the unlikely event an allergic reaction occurs, contact your doctor immediately. Symptoms include: difficulty breathing, fainting or dizziness, swelling. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Before using this drug, tell your doctor your medical history, including: allergies (especially drug allergies), blood disorders, severe high blood pressure, blood vessel or heart disease, skin rash/itching, intestinal problems (colitis), severe diabetes, lupus (SLE), cancer radiation treatment, urticaria, liver problems, kidney problems. This drug may cause sun sensitivity reactions (sunburn-like). Use sunscreens with UVA and B, and wear protective clothing. This medication should be used only when clearly needed during pregnancy. Discuss the risks and benefits with your doctor. This drug is excreted into breast milk. Because of the potential risk to the infant, breast-feeding while using this drug is not recommended. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Tell your doctor of all nonprescription and prescription medication you use, especially of: phenylbutazone, penicillamine, anti-cancer drugs, anti-malarials, immune suppression drugs (e.g., azathioprine). Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. Symptoms of overdose may include diarrhea, hives, and severe itching. NOTES: Laboratory tests will be done during therapy to reduce the chance of side effects. This drug may interfere with certain blood iodine tests. Do not share this medication with others. MISSED DOSE: If you miss a dose, consult your doctor or pharmacist promptly to establish a new dosing schedule. STORAGE: Store at room temperature between 59 and 86 degrees F (15-30 degrees C) away from light and moisture. Do not freeze. MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854-1166 (USA), or 1-800-668-1507 (Canada).
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Tagged Aurothioglucose, drug, information, intramusc, medication
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Auranofin oral
Auranofin oral
Drug Name Auranofin oral
Auranofin oral Drug Category AURANOFIN – ORAL
Auranofin oral Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. AURANOFIN – ORAL (awe-RAN-oh-fin) COMMON BRAND NAME(S): Ridaura WARNING: Rarely, this medication can cause severe (sometimes fatal) side effects including blood cell problems (decreased white blood cells and platelets). Immediately notify your doctor if you have signs of an infection (such as persistent sore throat or fever), unusual fatigue, dark or pink-reddish urine, itching, rash, mouth sores or irritation (stomatitis), or persistent diarrhea. Your doctor will be closely monitoring certain lab tests (e.g., white blood cells, platelets) before starting therapy and before you receive each injected dose or written prescription. USES: This medication is used to treat pain, swelling and stiffness associated with arthritis that is not controlled by other therapies. HOW TO USE: Take this medication as prescribed. Carefully read the patient package insert available with the product. Ask your doctor any questions you may have about this medication. It may take 3 to 4 months of therapy before the full benefits of this medication become apparent. SIDE EFFECTS: May cause stomach upset, nausea, loss of appetite, stomach cramps, gas, dizziness, weakness, sweating or flushing. If any of these effects persist or worsen, inform your doctor. Notify your doctor if you experience any of the following: mouth sores, sore throat, metallic taste in the mouth, nosebleeds, easy or unusual bleeding or bruising. Skin rash is common with this medication. If exposed to sunlight, skin may turn blue-grey in color. Avoid prolonged sun exposure and wear protective clothing. In the unlikely event you have an allergic reaction to this drug, seek immediate medical attention. Symptoms of an allergic reaction include: rash, itching, swelling, dizziness, trouble breathing. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Tell your doctor your medical history, especially: kidney or liver disease, bleeding problems or blood disorders, inflammatory bowel disease, colitis, rash, eczema, SLE (systemic lupus erythematosus), history of bone marrow depression, recent radiation therapy, any allergies. If you have a tuberculin (TB) skin test, tell the person performing the test that you take auranofin. This drug should be used only when clearly needed during pregnancy. Discuss the risks and benefits with your doctor. Injectable forms of auranofin are known to be excreted into breast milk. The manufacturer of this drug recommends you do not breast-feed while using this medication. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Tell your doctor of all prescription and nonprescription medications you may use, especially: other arthritis medications, phenytoin. Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. Symptoms of overdose may include hives and severe itching. NOTES: Do not allow anyone else to take your medication. It is important to maintain good oral hygiene while taking this medication. This medication can affect your blood. It is important to have regular check-ups and blood tests to monitor its effects. MISSED DOSE: If you miss a dose and are taking one dose daily, take it as soon as remembered unless you do not remember until the next day. In that case, skip the missed dose and resume your usual schedule. If you are taking more than one dose daily, take it as soon as remembered unless it is almost time for the next dose. In that case, skip the missed dose and resume your usual schedule. Do not double the dose to catch up. STORAGE: Store at room temperature between 59 and 86 degrees F (between 15 and 30 degrees C) away from moisture and sunlight. Do not store in the bathroom.
Attapulgite oral
Attapulgite oral
Drug Name Attapulgite oral
Attapulgite oral Drug Category ATTAPULGITE – ORAL
Attapulgite oral Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. ATTAPULGITE – ORAL (at-uh-PULL-gite) COMMON BRAND NAME(S): Diasorb, Donnagel, Kaopectate, Parepectolin USES: Attapulgite is used in the treatment of diarrhea. It works by absorbing fluid in the intestine. HOW TO USE: This medication is usually taken after each loose bowel movement. Follow package instructions. Chewable tablets must be chewed thoroughly before swallowing. The liquid form should be shaken well before pouring each dose. SIDE EFFECTS: This medication is generally well tolerated. Stomach upset may occur. If diarrhea is not relieved after two days of using this medication or you develop a fever or stomach cramps, notify your doctor. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Tell your doctor if you have: heart disease, bowel problems, allergies. This medication should be used only if clearly needed during pregnancy. Discuss the risks and benefits with your doctor. Consult your doctor before using any medication while breast-feeding. DRUG INTERACTIONS: Tell your doctor of any over-the-counter or prescription medication you may take. Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. NOTES: To maintain normal bowel habits, it is important to drink plenty of fluids (4-6 8 ounce glasses a day), eat foods high in fiber and roughage and exercise regularly. MISSED DOSE: If you miss a dose, take it as soon as remembered; do not take it if it is near the time for the next dose, instead, skip the missed dose and resume your usual dosing schedule. Do not “double-up” the dose to catch up. STORAGE: Store tablets at room temperature between 59 and 86 degrees F (15 to 30 degrees C) away from heat and light. The liquid form of this medication may be stored in the refrigerator to improve taste.
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Tagged Attapulgite, drug, information, medication, oral
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Atropine sulfate oral
Atropine sulfate oral
Drug Name Atropine sulfate oral
Atropine sulfate oral Drug Category ATROPINE – ORAL
Atropine sulfate oral Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. ATROPINE – ORAL (AT-trow-peen) COMMON BRAND NAME(S): Sal-Tropine USES: Atropine is used to treat a variety of stomach and intestinal tract disorders such as peptic ulcers, diarrhea, irritable bowel syndrome, diverticulitis, colitis, or pancreatitis. Atropine is also used to control bed-wetting and frequent urination, prevent motion sickness, treat alcohol withdrawal symptoms, Parkinson’s disease, asthma and poisonings due to certain insecticides or plants. HOW TO USE: Take this medication 30 minutes before meals. It is recommended to drink plenty of fluids while using this medication unless your doctor directs you otherwise. Take this medication as prescribed. Do not increase the dose or take it more frequently without consulting your doctor. SIDE EFFECTS: This medication may cause flushing of the face, problems sleeping, headache, blurred vision, drowsiness, increased sensitivity to light, constipation, dry mouth, reduced sweating or thirst. If these symptoms persist or worsen, notify your doctor. Notify your doctor if you develop: confusion, tremors, fast/irregular heartbeat, difficulty urinating. In the unlikely event you have an allergic reaction to this drug, seek immediate medical attention. Symptoms of an allergic reaction include: rash, itching, swelling, dizziness, trouble breathing. If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Tell your doctor your medical history, especially of: heart problems, glaucoma, stomach/abdominal/intestinal problems, prostate or urinary problems, contact lens wear, allergies (especially drug allergies). Because this medication can cause drowsiness, use caution when driving or performing tasks requiring alertness. Atropine reduces sweating which can lead to heat stroke in hot weather. Use caution engaging in strenuous activity during hot weather. Contact lens wearers may need to use appropriate lubricating solutions if this medication causes dry eyes. Elderly patients should use this medication with caution because they may be more sensitive to its effects. Children should use this medication with caution because they may be more sensitive to its effects. This medication should be used only when clearly needed during pregnancy. Discuss the risks and benefits with your doctor. Atropine may be excreted into breast milk. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Tell your doctor of all the medicines you may use (both prescription and nonprescription), especially of: antacids, digoxin, phenothiazines (e.g., chlopromazine), antihistamines (found in many cough/cold medicines), ketoconazole, potassium supplements, medications for Parkinson’s disease, certain heart medicines (e.g., disopyramide, procainamide, quinidine), tricyclic antidepressants (e.g., amitriptyline). Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. Symptoms of overdose may include: unusually dry mouth, excessive thirst, nausea, vomiting, difficulty breathing, blurred vision, dilated pupils, flushed/hot/dry skin, muscle weakness, unusual dizziness or drowsiness, restlessness, disorientation, seizures. seizures. NOTES: Do not share this medication with others. MISSED DOSE: If you miss a dose, take it as soon as remembered; do not take if it is almost time for the next dose, instead, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up. STORAGE: Store at room temperature away from sunlight and moisture. MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854-1166 (USA), or 1-800-668-1507 (Canada).
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Tagged Atropine, Atropine sulfate, drug, information, medication, oral
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Atropine sulfate ophthalmic
Atropine sulfate ophthalmic
Drug Name Atropine sulfate ophthalmic
Atropine sulfate ophthalmic Drug Category ATROPINE SULFATE – OPHTHALMIC
Atropine sulfate ophthalmic Drug Information
IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. ATROPINE SULFATE – OPHTHALMIC (AT-trow-peen, off-THAL-mick) COMMON BRAND NAME(S): Atropisol, Isopto Atropine USES: This medication relaxes muscles in the eye, which causes the pupil to widen (dilate). It is used to treat inflammation of certain parts of the eye (uveal tract). It is also used for certain eye exams. HOW TO USE: To apply eye drops, first wash your hands. Be careful not to touch the dropper or let it touch your eye or any other surface. Tilt your head back, gaze upward and pull down the lower eyelid to make a pouch. Place dropper directly over the eye and administer the prescribed number of drops. Look downward and gently close your eye for 1 or 2 minutes. Apply gentle pressure to the corner of the eye to keep the medicine in and to minimize the possibilty of the drug being absorbed by your body. Try not to blink and do not rub the eye. Do not rinse the dropper. If more than one type of eye medicine is to be used, wait at least 5 minutes before using other eye medications. Do not use eye drops that have changed color. SIDE EFFECTS: This medication may cause temporary drowsiness or blurred vision. Headache, temporary burning or stinging may occur at first. These effects should disappear as your body adjusts to this drug. If they persist or worsen, inform your doctor. This medication may cause your eyes to be sensitive to bright light. Wear sunglasses if needed. Unlikely but report changes in vision, eye pain, trembling, rapid heartbeat, fever, dizziness or difficult urination. In the unlikely event you have an allergic reaction to this drug, seek immediate medical attention. Symptoms of an allergic reaction include rash, itching, swelling, dizziness, breathing trouble or discharge from the eye(s). If you notice other effects not listed above, contact your doctor or pharmacist. PRECAUTIONS: Tell your doctor your medical history, especially: glaucoma (narrow angle), other eye problems, Down’s syndrome, any allergies. Do not wear soft contact lenses while using this drug because the lenses may discolor. Use caution when driving or performing tasks requiring alertness. Use caution when using this drug in children because children may be more sensitive to drug side effects. This medication should be used during pregnancy only if clearly needed. Discuss the risks and benefits with your doctor. It is not known if atropine eye medicine is excreted into breast milk. Consult your doctor before breast-feeding. DRUG INTERACTIONS: Before using this medicine, tell your doctor of all drugs you use (both prescription and nonprescription), especially of: other eye preparations. Do not start or stop any medicine without doctor or pharmacist approval. OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. This medicine may be harmful if swallowed. NOTES: Do not allow others to use this medication. MISSED DOSE: If you miss a dose, apply as soon as remembered; do not use if it is almost time for the next dose, instead, skip the missed dose and resume your usual dosing schedule. Do not “double-up” the dose to catch up. STORAGE: Store at room temperature between 59 and 86 degrees F (between 15 and 30 degrees C) away from moisture and sunlight. Do not store in the bathroom. Do not freeze this medication. Store solution in a cool, dark place. Discard the solution if it turns brown, cloudy or contains particles. When your doctor tells you to stop using this medication, throw away any unused portion. Do not save for later use.
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Tagged Atropine, Atropine sulfate, drug, information, medication, ophthalmic
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