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

CARDIAC ARREST ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
DYSPNOEA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
DEHYDRATION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RASH ( 3 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
MASS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
ULCER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
DYSURIA ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COMA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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