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Tricor (Fenofibrate) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (2)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Tricor (Fenofibrate) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Tricor side effects in male

Reported by a consumer/non-health professional from United States on 2012-05-07

Patient: male, weighing 85.7 kg (188.6 pounds)

Reactions: Renal Failure, Blood Potassium Increased, Thyroid Disorder, Diabetic Blindness

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Tricor
    Dosage: 145 mg, 1x/day
    Administration route: Oral
    Indication: Blood Cholesterol Increased

Glucotrol
    Dosage: 10 mg, daily
    Indication: Diabetes Mellitus
    Start date: 1998-01-01

Lipitor
    Indication: Cardiovascular Event Prophylaxis

Lipitor
    Indication: Myocardial Infarction

Trilipix
    Dosage: 45 mg, 1x/day
    Administration route: Oral
    Indication: Blood Cholesterol Increased

Lipitor
    Dosage: 40 mg, 1x/day
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 1998-01-01

Other drugs received by patient: Omega-3 Triglycerides; Vitamin D; Glucotrol XL; Januvia; Acetylsalicylic Acid; Coenzyme Q10; Calcium Carbonate / Famotidine / Magnesium Hydroxide



Possible Tricor side effects in 59 year old male

Reported by a consumer/non-health professional from United States on 2012-01-25

Patient: 59 year old male, weighing 120.2 kg (264.4 pounds)

Reactions: Pruritus, Respiratory Disorder, Urticaria, Headache, Abdominal Pain Upper, Dyspepsia, Cough, Epistaxis, White Blood Cell Count Decreased, Dyspnoea, Anaemia, Muscular Weakness, Renal Impairment, Diarrhoea, Throat Irritation, Arthralgia, Platelet Count Decreased, Asthenia

Adverse event resulted in: life threatening event, disablity

Drug(s) suspected as cause:
Tricor

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