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

PLATELET COUNT DECREASED ( 113 FDA reports)
PNEUMONIA ( 95 FDA reports)
PYREXIA ( 94 FDA reports)
ANAEMIA ( 71 FDA reports)
DIARRHOEA ( 63 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 62 FDA reports)
BLOOD CREATININE INCREASED ( 57 FDA reports)
BLOOD UREA INCREASED ( 57 FDA reports)
MALAISE ( 56 FDA reports)
NEUTROPHIL COUNT DECREASED ( 53 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 51 FDA reports)
INTERSTITIAL LUNG DISEASE ( 48 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 44 FDA reports)
LIVER DISORDER ( 44 FDA reports)
RASH ( 44 FDA reports)
SEPSIS ( 43 FDA reports)
HAEMOGLOBIN DECREASED ( 42 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 40 FDA reports)
THROMBOCYTOPENIA ( 38 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 37 FDA reports)
HAEMOPTYSIS ( 37 FDA reports)
DECREASED APPETITE ( 36 FDA reports)
NAUSEA ( 36 FDA reports)
HYPOGLYCAEMIA ( 34 FDA reports)
RENAL IMPAIRMENT ( 34 FDA reports)
DEHYDRATION ( 32 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 32 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 31 FDA reports)
RESPIRATORY FAILURE ( 31 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 30 FDA reports)
CONDITION AGGRAVATED ( 29 FDA reports)
VOMITING ( 29 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 29 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 28 FDA reports)
PANCYTOPENIA ( 28 FDA reports)
DEATH ( 26 FDA reports)
HYPOKALAEMIA ( 26 FDA reports)
CEREBRAL HAEMORRHAGE ( 25 FDA reports)
HYPERTENSION ( 25 FDA reports)
HYPOALBUMINAEMIA ( 25 FDA reports)
INFECTION ( 25 FDA reports)
VITREOUS HAEMORRHAGE ( 25 FDA reports)
PLEURAL EFFUSION ( 24 FDA reports)
BLOOD PRESSURE DECREASED ( 23 FDA reports)
CEREBRAL INFARCTION ( 23 FDA reports)
DYSPNOEA ( 23 FDA reports)
ERYTHEMA ( 23 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 23 FDA reports)
PURPURA ( 23 FDA reports)
HYPERKALAEMIA ( 21 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 20 FDA reports)
DISEASE PROGRESSION ( 20 FDA reports)
CARDIAC FAILURE ( 19 FDA reports)
CONSTIPATION ( 19 FDA reports)
NEOPLASM MALIGNANT ( 19 FDA reports)
OEDEMA PERIPHERAL ( 19 FDA reports)
RETINAL HAEMORRHAGE ( 19 FDA reports)
STOMATITIS ( 18 FDA reports)
BLOOD GLUCOSE INCREASED ( 17 FDA reports)
FEBRILE NEUTROPENIA ( 17 FDA reports)
HYPERGLYCAEMIA ( 17 FDA reports)
PAIN ( 17 FDA reports)
RHABDOMYOLYSIS ( 17 FDA reports)
SHOCK ( 17 FDA reports)
HYPOTHYROIDISM ( 16 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
HAEMATOCRIT DECREASED ( 15 FDA reports)
HYPERBILIRUBINAEMIA ( 15 FDA reports)
VISUAL ACUITY REDUCED ( 15 FDA reports)
BACK PAIN ( 14 FDA reports)
CHOLECYSTITIS ( 14 FDA reports)
HAEMATOCHEZIA ( 14 FDA reports)
PULMONARY HAEMORRHAGE ( 14 FDA reports)
ARRHYTHMIA ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 13 FDA reports)
COUGH ( 13 FDA reports)
LUNG NEOPLASM MALIGNANT ( 13 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
GASTROENTERITIS ( 12 FDA reports)
NEUTROPENIA ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
EPISTAXIS ( 11 FDA reports)
FEELING COLD ( 11 FDA reports)
FUNGAL INFECTION ( 11 FDA reports)
HAEMATURIA ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
LUNG DISORDER ( 11 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
POLLAKIURIA ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
CHILLS ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
EOSINOPHIL COUNT INCREASED ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
HYPOXIA ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
NEOPLASM PROGRESSION ( 10 FDA reports)
NEPHROTIC SYNDROME ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
BLOOD URIC ACID INCREASED ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
ENTERITIS ( 9 FDA reports)
ENTEROCOLITIS ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 9 FDA reports)
HYDROCEPHALUS ( 9 FDA reports)
INTESTINAL HAEMORRHAGE ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 9 FDA reports)
METASTASES TO LUNG ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
PERITONITIS ( 9 FDA reports)
ABDOMINAL DISCOMFORT ( 8 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
BURSITIS ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
INJECTION SITE OEDEMA ( 8 FDA reports)
INJECTION SITE PAIN ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
JEJUNAL ULCER ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
MALABSORPTION ( 8 FDA reports)
MELAENA ( 8 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 8 FDA reports)
PERIARTHRITIS ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
PHOTOSENSITIVITY REACTION ( 8 FDA reports)
RENAL ABSCESS ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
TINEA PEDIS ( 8 FDA reports)
ULCER ( 8 FDA reports)
URINE ABNORMALITY ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
ASCITES ( 7 FDA reports)
ASTHMA ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
METASTASES TO LYMPH NODES ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
NEUROSIS ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PERICARDITIS ( 7 FDA reports)
PYELONEPHRITIS ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CATARACT ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 6 FDA reports)
GENERALISED OEDEMA ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PERTUSSIS ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
PROSTATE CANCER ( 6 FDA reports)
PULMONARY NECROSIS ( 6 FDA reports)
RETINAL ISCHAEMIA ( 6 FDA reports)
RETINAL OEDEMA ( 6 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 6 FDA reports)
SERUM FERRITIN INCREASED ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
TENDERNESS ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EPIDERMOLYSIS BULLOSA ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
ILEUS ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 5 FDA reports)
PERITONITIS BACTERIAL ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
VITRECTOMY ( 5 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BONE MARROW TRANSPLANT ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
COMA ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTRIC CANCER STAGE IV ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTRITIS ATROPHIC ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HYPERTHERMIA MALIGNANT ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VESICAL FISTULA ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DUODENAL STENOSIS ( 3 FDA reports)
ENCEPHALITIS VIRAL ( 3 FDA reports)
ENDOPHTHALMITIS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FALL ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GENITAL HERPES ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPEREMESIS GRAVIDARUM ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
METASTASES TO ADRENALS ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATE CANCER STAGE IV ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RETINAL SCAR ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
URINE AMYLASE INCREASED ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER TAMPONADE ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
FEAR ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOBILIARY INFECTION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 2 FDA reports)
LEUKODERMA ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LYMPH NODE PALPABLE ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS FUNGAL ( 2 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYELOCYTE COUNT INCREASED ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PINEAL NEOPLASM ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATIC HAEMORRHAGE ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL MICROANEURYSMS ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETROPLACENTAL HAEMATOMA ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOOTH AVULSION ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URINARY SEDIMENT ABNORMAL ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR DRAINAGE ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY POSTOPERATIVE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD HYPOSMOSIS ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CHOROIDAL HAEMORRHAGE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP HAEMATOMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS HERPES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDIAL NEOPLASM ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
REITER'S SYNDROME ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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