effexor xr history
Like all antidepressants, Effexor could cause episodes of mania (abnormally high feelings of excitement and energy). Call your doctor at once if you have a serious Effexor side effect such as: seizure (convulsions); very stiff (rigid) muscles, high fever, sweating, confusion, fast or uneven heartbeats, tremors, feeling like you might pass effexor xr history agitation, hallucinations, fever, fast heart rate, overactive reflexes, nausea, vomiting, diarrhea, loss of coordination; headache, trouble concentrating, memory problems, weakness, feeling unsteady, confusion, hallucinations, fainting, shallow breathing or breathing that stops; cough, chest tightness, trouble breathing; or easy bruising. The clinical relevance of this finding for hypertensive patients is unknown. Clinically relevant increases in serum cholesterol, defined as 1) a final on-therapy increase in serum cholesterol ≥50 mg/dL from baseline and to a value ≥261 mg/dL or 2) an average on‑therapy increase in serum cholesterol ≥50 mg/dL from baseline and to a value ≥261 mg/dL, were recorded in 5.3% of venlafaxine-treated patients and 0.0% of placebo-treated patients (see PRECAUTIONS-General-Serum Cholesterol Elevation). Antidepressant medicines may increase suicidal thoughts or actions in some children, teenagers, and young adults within the first few months of treatment. Screening Patients for Bipolar Disorder A major depressive episode may be the initial presentation of bipolar disorder. The follow-up period to observe patients for relapse, defined as a CGI Severity of Illness item score ≥4, was for up effexor xr history 52 weeks. Venlafaxine hydrochloride is a white to off-white crystalline solid with a solubility of 572 mg/mL in water (adjusted to ionic strength of 0.2 M with sodium chloride). Ask your doctor before taking any medicine for pain, arthritis, fever, or swelling. Effexor should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed. When increasing the dose, increments of up to 75 mg/day should be made at intervals of no less than 4 days. Overdose symptoms may include vomiting, fast heart rate, blurred vision, extreme drowsiness, or seizure (convulsions). Unit of Use 20 Tablets Rx only Wyeth® Effexor venlafaxine hydrochloride tablet Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0008-0701 Route effexor xr history effexor xr history ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 25 mg Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED LACTOSE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO POWDERED CELLULOSE Product Characteristics Color ORANGE (PEACH) Score 2 pieces Shape PENTAGON (5 sided) (SHIELD-SHAPED) Size 6mm Flavor Imprint Code 25;W;701 Contains Packaging # NDC Package Description Multilevel Packaging 1 0008-0701-08 60 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020151 12/01/1993 Effexor venlafaxine hydrochloride tablet Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0008-0781 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 37.5 mg Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED LACTOSE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO POWDERED CELLULOSE Product Characteristics Color ORANGE (PEACH) Score 2 pieces Shape PENTAGON (5 sided) (SHIELD-SHAPED) Size 7mm Flavor Imprint Code 375;W;781 Contains Packaging # NDC Package Description Multilevel Packaging 1 0008-0781-08 60 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020151 12/01/1993 Effexor venlafaxine hydrochloride tablet Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0008-0703 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 50 mg Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED LACTOSE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO POWDERED CELLULOSE Product Characteristics Color ORANGE (PEACH) Score 2 pieces Shape PENTAGON (5 sided) (SHIELD-SHAPED) Size 8mm Flavor Imprint Code 50;W;703 Contains Packaging # NDC Package Description Multilevel Packaging 1 0008-0703-07 30 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020151 12/01/1993 Effexor venlafaxine hydrochloride tablet Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0008-0704 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) effexor xr history 75 mg Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED LACTOSE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO POWDERED CELLULOSE Product Characteristics Color ORANGE (PEACH) Score 2 pieces Shape PENTAGON (5 sided) (SHIELD-SHAPED) Size 9mm Flavor Imprint Code 75;W;704 Contains Packaging # NDC Package Description Multilevel Packaging 1 0008-0704-07 30 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020151 12/01/1993 Effexor venlafaxine hydrochloride tablet Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0008-0705 Route of effexor xr history ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 100 mg effexor xr history Ingredients Ingredient Name Strength FERRIC OXIDE RED LACTOSE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A effexor xr history POWDERED CELLULOSE Product Characteristics Color ORANGE (PEACH) Score 2 pieces Shape PENTAGON (5 sided) (SHIELD-SHAPED) Size 10mm Flavor Imprint Code 100;W;705 Contains Packaging # NDC Package Description Multilevel Packaging 1 0008-0705-07 20 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020151 12/01/1993 Labeler - Wyeth Pharmaceuticals Company (071170729) Establishment Name Address ID/FEI Operations Wyeth Pharmaceuticals Company 071170729 MANUFACTURE, ANALYSIS Revised: 01/2010Wyeth Pharmaceuticals Company Effexor effexor xr history name: Venlafaxine hydrochloride Brand names: Effexor XR, Effexor Why is Effexor prescribed? Effexor is prescribed for the treatment of depression—that is, a continuing depression that interferes with daily functioning. 3. Take Effexor by mouth with food. Indinavir—In a study of 9 healthy volunteers, venlafaxine administered under steady-state conditions at 150 mg/day resulted in a 28% decrease in the AUC of a single 800 mg oral dose of indinavir and a 36% decrease in indinavir Cmax. Cimetidine Concomitant administration of cimetidine and venlafaxine in a steady-state study for both drugs resulted in inhibition of first-pass metabolism of venlafaxine in 18 healthy subjects. Effexor may be harmful to an unborn baby, and may cause problems in a newborn baby if the mother takes the medication late in pregnancy (during the third trimester). The complete text of the Medication Guide is reprinted at the end effexor xr history this document. This includes aspirin, ibuprofen (Advil, Motrin), naproxen (Aleve, Naprosyn), diclofenac (Voltaren), indomethacin, piroxicam (Feldene), nabumetone (Relafen), etodolac (Lodine), and others. effexor xr history may include agitation; confusion; hallucinations; coma; fever; fast or irregular heartbeat; tremor; excessive sweating; and nausea, vomiting, or diarrhea.
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