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

HAEMORRHAGE INTRACRANIAL ( 35 FDA reports)
DEATH ( 28 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
ANAL ATRESIA ( 11 FDA reports)
BLADDER AGENESIS ( 11 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 11 FDA reports)
EXOMPHALOS ( 11 FDA reports)
GASTROINTESTINAL MALFORMATION ( 11 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
VIRAL LOAD INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HIV INFECTION ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
AIDS DEMENTIA COMPLEX ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 5 FDA reports)
CEREBELLAR ATAXIA ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
SUBCUTANEOUS ABSCESS ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 4 FDA reports)
EATON-LAMBERT SYNDROME ( 4 FDA reports)
ENCEPHALITIS VIRAL ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
RASH ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
END STAGE AIDS ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FALL ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPHAEMA ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL APLASTIC ANAEMIA ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VIRAL LOAD ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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