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PHARMACEUTICAL PRODUCT COMPLAINT ( 2363 FDA reports)
ADVERSE EVENT ( 2206 FDA reports)
HIV INFECTION ( 589 FDA reports)
HEPATITIS C VIRUS ( 465 FDA reports)
HEPATITIS C ( 275 FDA reports)
HIV TEST POSITIVE ( 80 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 76 FDA reports)
FACTOR VIII INHIBITION ( 48 FDA reports)
HEPATITIS C POSITIVE ( 36 FDA reports)
HAEMORRHAGE ( 25 FDA reports)
HEPATITIS B ( 25 FDA reports)
DIARRHOEA ( 22 FDA reports)
HEPATITIS B VIRUS ( 22 FDA reports)
UNEVALUABLE EVENT ( 22 FDA reports)
HEPATITIS A ( 17 FDA reports)
ANAEMIA ( 16 FDA reports)
RASH ( 16 FDA reports)
HYPOTENSION ( 15 FDA reports)
HAEMATOMA ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
DEATH ( 13 FDA reports)
HEPATIC CIRRHOSIS ( 13 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
HAEMATURIA ( 11 FDA reports)
HEPATITIS NON-A NON-B ( 11 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
MONOCYTE COUNT INCREASED ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
DEPRESSION ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ACUTE ABDOMEN ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
PAIN ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
FALL ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INJURY ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
INDIRECT INFECTION TRANSMISSION ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
VOMITING ( 4 FDA reports)
VON WILLEBRAND'S DISEASE ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 3 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HTLV-1 TEST POSITIVE ( 2 FDA reports)
HTLV-2 TEST POSITIVE ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RALES ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
STRESS ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TROPICAL SPASTIC PARESIS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE HIV INFECTION ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYST ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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