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

RENAL FAILURE ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
DEPRESSION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
PARAPLEGIA ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
PAIN ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
STRESS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
INJURY ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
CRYING ( 2 FDA reports)
FEAR ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
COUGH ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)

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