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

PYREXIA ( 90 FDA reports)
RASH ( 50 FDA reports)
PLATELET COUNT DECREASED ( 47 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 45 FDA reports)
LIVER DISORDER ( 40 FDA reports)
MALAISE ( 38 FDA reports)
INTERSTITIAL LUNG DISEASE ( 36 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 35 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 34 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 33 FDA reports)
VOMITING ( 31 FDA reports)
BLOOD CREATININE INCREASED ( 29 FDA reports)
EOSINOPHIL COUNT INCREASED ( 28 FDA reports)
PNEUMONIA ( 27 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 26 FDA reports)
NASOPHARYNGITIS ( 25 FDA reports)
ERYTHEMA MULTIFORME ( 24 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
RHABDOMYOLYSIS ( 23 FDA reports)
WEIGHT INCREASED ( 23 FDA reports)
ERYTHEMA ( 22 FDA reports)
RENAL IMPAIRMENT ( 22 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 22 FDA reports)
ANAEMIA ( 20 FDA reports)
ANOREXIA ( 20 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 20 FDA reports)
COUGH ( 20 FDA reports)
DRUG ERUPTION ( 20 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 19 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 19 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 18 FDA reports)
BLOOD PRESSURE DECREASED ( 18 FDA reports)
ATRIAL FIBRILLATION ( 17 FDA reports)
DIZZINESS ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
HAEMOGLOBIN DECREASED ( 17 FDA reports)
NAUSEA ( 17 FDA reports)
PALPITATIONS ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
CARDIAC FAILURE ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
PRURITUS ( 16 FDA reports)
RENAL FAILURE ( 16 FDA reports)
ASTHMA ( 15 FDA reports)
DIARRHOEA ( 15 FDA reports)
DYSPNOEA ( 15 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
ASTHENIA ( 14 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 14 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
DYSARTHRIA ( 14 FDA reports)
HERPES ZOSTER ( 14 FDA reports)
JAUNDICE ( 14 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 14 FDA reports)
BLOOD POTASSIUM INCREASED ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 13 FDA reports)
PULMONARY CONGESTION ( 13 FDA reports)
BLOOD POTASSIUM DECREASED ( 12 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
PAIN ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
STOMATITIS ( 12 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
ECZEMA ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
METABOLIC ACIDOSIS ( 11 FDA reports)
MYALGIA ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
EOSINOPHILIA ( 10 FDA reports)
GAIT DISTURBANCE ( 10 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 10 FDA reports)
PEMPHIGOID ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
BRADYCARDIA ( 9 FDA reports)
CHOLELITHIASIS ( 9 FDA reports)
DIZZINESS POSTURAL ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
MELAENA ( 9 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 9 FDA reports)
MYOGLOBINURIA ( 9 FDA reports)
SHOCK ( 9 FDA reports)
ALOPECIA ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DYSPNOEA EXACERBATED ( 8 FDA reports)
FALL ( 8 FDA reports)
GRANULOCYTE COUNT DECREASED ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
ORTHOPNOEA ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PNEUMOTHORAX ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
THYROID CANCER ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 6 FDA reports)
DERMATOMYOSITIS ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
FACIAL PALSY ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
JAUNDICE CHOLESTATIC ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ENANTHEMA ( 5 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 5 FDA reports)
HAEMORRHAGIC DISORDER ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PULMONARY FIBROSIS ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CREATININE URINE INCREASED ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIABETIC NEPHROPATHY ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GASTRITIS ATROPHIC ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RHEUMATOID LUNG ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SURGERY ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WALKING DISABILITY ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CYTOREDUCTIVE SURGERY ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HEPATIC ATROPHY ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MEDIASTINITIS ( 3 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 3 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
SELECTIVE ABORTION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URINE AMYLASE INCREASED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
X-RAY ABNORMAL ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROENTERITIS RADIATION ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PERICORONITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INFLUENZA SEROLOGY ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FISTULA ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THIRST ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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