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PULMONARY EMBOLISM ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ANGER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ACNE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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