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

PYREXIA ( 47 FDA reports)
CHOLESTASIS ( 33 FDA reports)
THROMBOCYTOPENIA ( 32 FDA reports)
OEDEMA PERIPHERAL ( 29 FDA reports)
RENAL FAILURE ACUTE ( 28 FDA reports)
PRURITUS ( 26 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 22 FDA reports)
PANCYTOPENIA ( 22 FDA reports)
PURPURA ( 22 FDA reports)
RASH ( 21 FDA reports)
JAUNDICE ( 20 FDA reports)
SEPTIC SHOCK ( 20 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
TOXIC SKIN ERUPTION ( 19 FDA reports)
CONVULSION ( 17 FDA reports)
COMA ( 16 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 16 FDA reports)
CYTOLYTIC HEPATITIS ( 15 FDA reports)
ERYTHEMA ( 15 FDA reports)
LIVER DISORDER ( 15 FDA reports)
METABOLIC ACIDOSIS ( 15 FDA reports)
RASH MACULO-PAPULAR ( 15 FDA reports)
SKIN EXFOLIATION ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
HYPERTHERMIA ( 14 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
EOSINOPHILIA ( 13 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
HEPATOMEGALY ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
CEREBELLAR SYNDROME ( 12 FDA reports)
CONFUSIONAL STATE ( 12 FDA reports)
GASTROINTESTINAL DISORDER ( 12 FDA reports)
HEPATITIS CHOLESTATIC ( 12 FDA reports)
NEUTROPENIA ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BALANCE DISORDER ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
FACE OEDEMA ( 10 FDA reports)
HEPATOCELLULAR DAMAGE ( 10 FDA reports)
LYMPHADENOPATHY ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
ANURIA ( 9 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 9 FDA reports)
HEPATITIS ( 9 FDA reports)
INTENTIONAL DRUG MISUSE ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
TREMOR ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
DECEREBRATION ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
EYE MOVEMENT DISORDER ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
LYMPHADENITIS ( 8 FDA reports)
MALNUTRITION ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
RASH MORBILLIFORM ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
STATUS EPILEPTICUS ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
BLAST CELL COUNT INCREASED ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
APLASIA ( 6 FDA reports)
BLISTER ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
FEBRILE BONE MARROW APLASIA ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ALVEOLITIS ( 5 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
COUGH ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
GAMMOPATHY ( 5 FDA reports)
HEPATIC FIBROSIS ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PERITONEAL EFFUSION ( 5 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
VASCULAR PURPURA ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG LEVEL DECREASED ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
FISTULA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COAGULATION FACTOR DECREASED ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
RALES ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CROSS SENSITIVITY REACTION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MYCOTIC ANEURYSM ( 1 FDA reports)
NEONATAL ANURIA ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE ELECTROLYTES ABNORMAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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