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

LOSS OF CONSCIOUSNESS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
FALL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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