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

PYREXIA ( 30 FDA reports)
CHOLESTASIS ( 24 FDA reports)
SEPTIC SHOCK ( 20 FDA reports)
RENAL FAILURE ACUTE ( 18 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
AGRANULOCYTOSIS ( 15 FDA reports)
CYTOLYTIC HEPATITIS ( 14 FDA reports)
RENAL FAILURE ( 14 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
RASH ( 12 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
BONE MARROW FAILURE ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
TOXIC SKIN ERUPTION ( 10 FDA reports)
CHILLS ( 9 FDA reports)
DERMATITIS BULLOUS ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
PURPURA ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
APLASIA ( 7 FDA reports)
ASCITES ( 7 FDA reports)
DEATH ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CELL DEATH ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MALAISE ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ACINETOBACTER INFECTION ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
COMA ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MONONUCLEOSIS SYNDROME ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SHOCK ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ATELECTASIS ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GAMMOPATHY ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ARTHRITIS FUNGAL ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOGLOBULINAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APOLIPOPROTEIN INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRAIN STEM THROMBOSIS ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
FALL ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOPORPHYRIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PITUITARY GLAND ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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