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

DRUG INEFFECTIVE ( 6 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
COUGH ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
LIPODYSTROPHY ACQUIRED ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
GENOTYPE DRUG RESISTANCE TEST ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITOCHONDRIAL DNA DELETION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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