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

HYPOTENSION ( 14 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
OPSOCLONUS MYOCLONUS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DELUSION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
ANURIA ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
FALL ( 2 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
DEATH ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
COUGH ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)

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