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

PYREXIA ( 60 FDA reports)
RENAL FAILURE ACUTE ( 39 FDA reports)
THROMBOCYTOPENIA ( 36 FDA reports)
FEBRILE BONE MARROW APLASIA ( 34 FDA reports)
CYTOLYTIC HEPATITIS ( 31 FDA reports)
COMA ( 29 FDA reports)
CONFUSIONAL STATE ( 27 FDA reports)
PANCYTOPENIA ( 27 FDA reports)
CEREBELLAR SYNDROME ( 26 FDA reports)
CONVULSION ( 26 FDA reports)
BONE MARROW FAILURE ( 25 FDA reports)
MYDRIASIS ( 25 FDA reports)
CARDIO-RESPIRATORY ARREST ( 22 FDA reports)
CHOLESTASIS ( 22 FDA reports)
DIARRHOEA ( 22 FDA reports)
LUNG DISORDER ( 22 FDA reports)
PANCREATITIS ACUTE ( 22 FDA reports)
PLEURAL EFFUSION ( 22 FDA reports)
ABDOMINAL PAIN ( 21 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 21 FDA reports)
RENAL FAILURE ( 21 FDA reports)
SEPSIS ( 21 FDA reports)
BLOOD BILIRUBIN INCREASED ( 19 FDA reports)
TOXIC SKIN ERUPTION ( 19 FDA reports)
APLASIA ( 18 FDA reports)
DERMATITIS EXFOLIATIVE ( 18 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 18 FDA reports)
PNEUMONIA ( 18 FDA reports)
TACHYPNOEA ( 18 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 18 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
EYE MOVEMENT DISORDER ( 17 FDA reports)
HYPERTHERMIA ( 17 FDA reports)
HYPOTENSION ( 17 FDA reports)
SINUS BRADYCARDIA ( 17 FDA reports)
VENTRICULAR FIBRILLATION ( 17 FDA reports)
VOMITING ( 17 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
LIVER DISORDER ( 16 FDA reports)
DECEREBRATION ( 15 FDA reports)
JAUNDICE ( 15 FDA reports)
MUCOSAL INFLAMMATION ( 15 FDA reports)
RESPIRATORY DISTRESS ( 15 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
HYPERNATRAEMIA ( 14 FDA reports)
INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
LYMPHADENITIS ( 14 FDA reports)
STEM CELL TRANSPLANT ( 14 FDA reports)
DERMATITIS BULLOUS ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
STAPHYLOCOCCAL INFECTION ( 13 FDA reports)
ARRHYTHMIA ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
BLAST CELL COUNT INCREASED ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
HEPATOMEGALY ( 10 FDA reports)
HYPERBILIRUBINAEMIA ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
AGITATION ( 9 FDA reports)
ANAEMIA ( 9 FDA reports)
ASCITES ( 9 FDA reports)
FEBRILE NEUTROPENIA ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
PREMATURE BABY ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
SKIN INFLAMMATION ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
VASCULITIS CEREBRAL ( 8 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
HEPATIC STEATOSIS ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
SHOCK ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHILLS ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEATH ( 6 FDA reports)
ENTEROCOCCAL INFECTION ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
GASTRIC MUCOSAL LESION ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
JAUNDICE NEONATAL ( 6 FDA reports)
MALAISE ( 6 FDA reports)
NIKOLSKY'S SIGN ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
OPTIC NEUROPATHY ( 6 FDA reports)
PAIN OF SKIN ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BONE MARROW TRANSPLANT ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CRYING ( 5 FDA reports)
CSF PROTEIN INCREASED ( 5 FDA reports)
CULTURE STOOL POSITIVE ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 5 FDA reports)
RASH ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 4 FDA reports)
ANURIA ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
CAPNOCYTOPHAGIA INFECTION ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
CYTOTOXIC OEDEMA ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
ENTERAL NUTRITION ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CRANIAL NERVE PARALYSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DELAYED PUBERTY ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FACTOR V DEFICIENCY ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FOETAL HEART RATE DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PERITONEAL EFFUSION ( 3 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 2 FDA reports)
APPLICATION SITE PARAESTHESIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
DECREASED VIBRATORY SENSE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEONATAL CHOLESTASIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEURALGIC AMYOTROPHY ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATOFIBROSARCOMA ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHROBLAST MORPHOLOGY ABNORMAL ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASS ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)

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