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

CARDIAC FAILURE ( 5 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
NAUSEA ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MALAISE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CHEST PAIN ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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