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

PLATELET COUNT DECREASED ( 28 FDA reports)
DIARRHOEA ( 27 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 23 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 23 FDA reports)
PYREXIA ( 23 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 18 FDA reports)
CONDITION AGGRAVATED ( 18 FDA reports)
VOMITING ( 18 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
NAUSEA ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
RASH ( 16 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
FALL ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
MALAISE ( 11 FDA reports)
NASOPHARYNGITIS ( 11 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
COMA ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
PAIN ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
MULTIPLE MYELOMA ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
SHOCK ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
INGROWING NAIL ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DISSOCIATIVE FUGUE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MANIA ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
NEUROBLASTOMA RECURRENT ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SINUSITIS ASPERGILLUS ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SCEDOSPORIUM INFECTION ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THIRST ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
COXSACKIE VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDODIVERTICULAR DISEASE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)

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