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

CEREBRAL ARTERY THROMBOSIS ( 58 FDA reports)
DEEP VEIN THROMBOSIS ( 58 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 55 FDA reports)
PORTAL VEIN THROMBOSIS ( 55 FDA reports)
CATHETER THROMBOSIS ( 54 FDA reports)
RENAL VEIN THROMBOSIS ( 54 FDA reports)
HAEMORRHAGE ( 53 FDA reports)
FEBRILE NEUTROPENIA ( 44 FDA reports)
NEUTROPENIA ( 41 FDA reports)
PYREXIA ( 40 FDA reports)
CONVULSION ( 37 FDA reports)
ADENOVIRAL HEPATITIS ( 35 FDA reports)
COAGULOPATHY ( 33 FDA reports)
HEMIPLEGIA ( 33 FDA reports)
MUCOSAL INFLAMMATION ( 32 FDA reports)
DIARRHOEA ( 29 FDA reports)
RENAL FAILURE ( 28 FDA reports)
GLIOMA ( 27 FDA reports)
HYPERTENSION ( 27 FDA reports)
HEPATIC ENCEPHALOPATHY ( 26 FDA reports)
PNEUMONIA ( 26 FDA reports)
THROMBOSIS ( 26 FDA reports)
ABDOMINAL PAIN ( 24 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 24 FDA reports)
HYPOTENSION ( 24 FDA reports)
HEPATOTOXICITY ( 23 FDA reports)
HEPATIC FAILURE ( 22 FDA reports)
HEPATOMEGALY ( 22 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 21 FDA reports)
HEPATIC STEATOSIS ( 21 FDA reports)
THROMBOCYTOPENIA ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
BLOOD BILIRUBIN INCREASED ( 20 FDA reports)
RETINAL VEIN THROMBOSIS ( 19 FDA reports)
STAPHYLOCOCCAL INFECTION ( 19 FDA reports)
VOMITING ( 19 FDA reports)
BLINDNESS UNILATERAL ( 18 FDA reports)
CHOLESTASIS ( 18 FDA reports)
EYE PAIN ( 18 FDA reports)
LEUKOENCEPHALOPATHY ( 18 FDA reports)
PAPILLOEDEMA ( 18 FDA reports)
PLEURAL EFFUSION ( 18 FDA reports)
BACTERIAL SEPSIS ( 17 FDA reports)
HYPONATRAEMIA ( 17 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 17 FDA reports)
ASCITES ( 16 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 16 FDA reports)
FEBRILE BONE MARROW APLASIA ( 16 FDA reports)
GASTRITIS ( 16 FDA reports)
HYPERGLYCAEMIA ( 16 FDA reports)
ILEUS PARALYTIC ( 16 FDA reports)
NEUROTOXICITY ( 16 FDA reports)
OFF LABEL USE ( 16 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 16 FDA reports)
ASTHENIA ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
ZYGOMYCOSIS ( 15 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
PSEUDOMONAS INFECTION ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 13 FDA reports)
CEREBRAL ISCHAEMIA ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
HEPATITIS ACUTE ( 13 FDA reports)
IRRITABILITY ( 13 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
CANDIDA SEPSIS ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
COMA ( 12 FDA reports)
HERPES SIMPLEX ( 12 FDA reports)
HYPERNATRAEMIA ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
PARALYSIS ( 12 FDA reports)
RASH ( 12 FDA reports)
VENOUS THROMBOSIS ( 12 FDA reports)
BLINDNESS ( 11 FDA reports)
COLITIS ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
ENCEPHALITIC INFECTION ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
SEPTIC SHOCK ( 11 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 11 FDA reports)
AREFLEXIA ( 10 FDA reports)
BONE MARROW FAILURE ( 10 FDA reports)
CEREBRAL HAEMORRHAGE ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
ENCEPHALOPATHY ( 10 FDA reports)
FUNGAL INFECTION ( 10 FDA reports)
HEPATIC NECROSIS ( 10 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 10 FDA reports)
LIVER ABSCESS ( 10 FDA reports)
PANCYTOPENIA ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
CAECITIS ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DERMATITIS BULLOUS ( 9 FDA reports)
HEMIPARESIS ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
HYPOPROTEINAEMIA ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
METASTASIS ( 9 FDA reports)
NEOPLASM MALIGNANT ( 9 FDA reports)
OPTIC NEURITIS ( 9 FDA reports)
PAIN OF SKIN ( 9 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
THERAPY NON-RESPONDER ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
ANAPHYLACTIC REACTION ( 8 FDA reports)
BLOOD CULTURE POSITIVE ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
GASTRIC MUCOSAL LESION ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HYPOPHOSPHATAEMIA ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
MECHANICAL VENTILATION ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
NIKOLSKY'S SIGN ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
RESPIRATORY TRACT INFECTION ( 8 FDA reports)
SKIN EROSION ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 8 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
INTUSSUSCEPTION ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
PNEUMONITIS ( 7 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 7 FDA reports)
SYSTEMIC CANDIDA ( 7 FDA reports)
ADENOVIRUS INFECTION ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CATHETER RELATED INFECTION ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 6 FDA reports)
COMA HEPATIC ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
DYSTONIA ( 6 FDA reports)
ENTERAL NUTRITION ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 6 FDA reports)
INFECTION ( 6 FDA reports)
JAUNDICE CHOLESTATIC ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
LYMPHANGITIS ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CANDIDA PNEUMONIA ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
COUGH ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
FALL ( 5 FDA reports)
GUILLAIN-BARRE SYNDROME ( 5 FDA reports)
HEPATIC HAEMORRHAGE ( 5 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
MALIGNANT GLIOMA ( 5 FDA reports)
MENTAL IMPAIRMENT ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
MUTISM ( 5 FDA reports)
NECROTISING COLITIS ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
TREMOR ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
APLASIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
FUSARIUM INFECTION ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAPTOGLOBIN DECREASED ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OESOPHAGEAL STENOSIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
SALIVARY GLAND CANCER ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
TRICHOSPORON INFECTION ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
AMIMIA ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 3 FDA reports)
CHORIORETINAL ATROPHY ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CRANIAL NERVE INJURY ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EXTERNAL EAR PAIN ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
FACIAL NERVE DISORDER ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOFIBRINOGENAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MANIA ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PSEUDOBULBAR PALSY ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
RETINAL DYSTROPHY ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SCROTAL INFECTION ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABSCESS FUNGAL ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CEREBRAL HYGROMA ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROSCLEROSIS ( 2 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CYTOLOGY ABNORMAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
FUNGUS URINE TEST POSITIVE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PUNCTURE SITE INFECTION ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMYLASE ABNORMAL ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD GALACTOSE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRONCHIAL ULCERATION ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA REFRACTORY ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAT ATROPHY ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GASTROENTERITIS PSEUDOMONAS ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MENINGEAL LEUKAEMIA ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOXANTHOMA ELASTICUM ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REFRACTORY CANCER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
SALIVARY GLAND CANCER RECURRENT ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC INFECTION FUNGAL ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRICHOSTASIS SPINULOSA ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UROGENITAL INFECTION FUNGAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)

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