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TEMODAR 140 mg: lactose anhydrous (246 mg), colloidal silicon dioxide (0.4 mg), sodium starch glycolate (21 mg), tartaric acid (4.2 mg), and stearic acid (8.4 mg).

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Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney problems, liver problems, decreased bone marrow function, blood cell disorders (e.g., anemia, leukopenia, thrombocyenia). What are the possible side effects of amphetamine and dextroamphetamine (Adderall, Adderall XR)

Why Diclofenac Sodium EC should not be prescribed Diclofenac Sodium EC should not be used by people in whom aspirin or other NSAIDs, eg ibuprofen, cause allergic reactions such as asthma attacks, itchy rash (urticaria), nasal inflammation (rhinitis) or swelling of the lips, tongue and throat (angioedema) Diclofenac Sodium EC should not be used if you have a history of bleeding from the stomach or intestines. Diclofenac Sodium EC should not be used if suspect or have a history of Peptic ulcer. Diclofenac Sodium EC should not be used if you are allergic to one or any of its ingredients. Please inform your doctor or pharmacist if you have previously experienced such an allergy. If you feel you have experienced an allergic reaction, s using Diclofenac Sodium EC and inform your doctor or pharmacist immediately. Possible Diclofenac Sodium EC Side effects More common side effects of Diclofenac Sodium EC may include: abdominal pain or cramps, constipation, diarrhea, headache, indigestion, nausea Less common side effects of Diclofenac Sodium EC may include: abdominal bleeding, abdominal swelling, dizziness, fluid retention, gas, itching, peptic ulcers, rash, ringing in the ears Rare side effects of Diclofenac Sodium EC may include: anaphylaxis (severe allergic reaction), anemia, anxiety, appetite change, asthma, black stools, blood disorders, bloody diarrhea, blurred vision, changes in taste, colitis, congestive heart failure, convulsions, decrease in white blood cells, decreased urine production, depression, double vision, drowsiness, dry mouth and mucous membranes, hair loss, hearing loss, hepatitis, high blood pressure, hives, inability to sleep, inflammation of the colon, inflammation of mouth, inflammation of the pancreas, irritability, kidney failure, liver disease, low blood pressure, nosebleed, red or purple skin discoloration and itching, sensitivity to light, skin eruptions and inflammation, scaling or peeling, sores in the gullet, Stevens-Johnson syndrome (a severe form of skin eruption), swelling of eyelids, lips, and tongue, swelling of the throat due to fluid retention, vague feeling of illness, vision changes, vomiting, yellow eyes and skin Holiday Depression and Stress

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The adsorbed diphtheria, tetanus and acellular pertussis components are combined with aluminum phosphate (as adjuvant), 2-phenoxyethanol (not as a preservative) and water for injection.Blood thinning agents such as Coumadin, Fluconazole (Diflucan), Furosemide (Lasix), Lithium (Eskalith, Lithobid), Inactive Ingredients

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LEVAQUIN Injection in Single-Use Vials is a sterile, preservative-free aqueous solution of levofloxacin in Water for Injection, with pH ranging from 3.8 to 5.8. MISSED DOSE: If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Each mL of COMBIGAN contains the active ingredients brimonidine tartrate 0.2% and timolol 0.5% with the inactive ingredients benzalkonium chloride 0.005%; sodium phosphate, monobasic; sodium phosphate, dibasic; purified water; and hydrochloric acid and/or sodium hydroxide to adjust pH.

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