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

ABNORMAL BEHAVIOUR ( 34 FDA reports)
PYREXIA ( 25 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 18 FDA reports)
HAEMATOCHEZIA ( 13 FDA reports)
HALLUCINATION ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
CHROMATURIA ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
PALLOR ( 12 FDA reports)
CONVULSION ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
PAIN ( 6 FDA reports)
SHOCK ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
FALL ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
MOANING ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SUBACUTE HEPATIC FAILURE ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FEAR ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERURICOSURIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
AGITATION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ENCEPHALITIS INFLUENZAL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEUROBLASTOMA RECURRENT ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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