Please choose an event type to view the corresponding MedsFacts report:

HEPATITIS ( 5 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)

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