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

CONFUSIONAL STATE ( 7 FDA reports)
PYREXIA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
AGITATION ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC MASSAGE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MICROSPORUM INFECTION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APLASIA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
SHOCK ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)

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