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

COMPLETED SUICIDE ( 7 FDA reports)
DEATH ( 6 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
POISONING ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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