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

CARDIAC FAILURE ( 65 FDA reports)
PLATELET COUNT DECREASED ( 60 FDA reports)
ANAEMIA ( 49 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 44 FDA reports)
RENAL IMPAIRMENT ( 44 FDA reports)
DECREASED APPETITE ( 42 FDA reports)
MALAISE ( 40 FDA reports)
PYREXIA ( 40 FDA reports)
DIARRHOEA ( 35 FDA reports)
PLEURAL EFFUSION ( 31 FDA reports)
PNEUMONIA ( 29 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 29 FDA reports)
NAUSEA ( 28 FDA reports)
DEHYDRATION ( 27 FDA reports)
INTERSTITIAL LUNG DISEASE ( 27 FDA reports)
VOMITING ( 26 FDA reports)
LIVER DISORDER ( 23 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 23 FDA reports)
STEVENS-JOHNSON SYNDROME ( 23 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
ATRIAL FIBRILLATION ( 22 FDA reports)
NEUTROPHIL COUNT DECREASED ( 22 FDA reports)
BLOOD CREATININE INCREASED ( 21 FDA reports)
OEDEMA ( 21 FDA reports)
RENAL FAILURE ( 21 FDA reports)
SEPSIS ( 21 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 20 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 20 FDA reports)
DYSPNOEA ( 20 FDA reports)
RASH ( 20 FDA reports)
BLOOD BILIRUBIN INCREASED ( 19 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 19 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 19 FDA reports)
HYPERKALAEMIA ( 18 FDA reports)
HYPERTENSION ( 18 FDA reports)
OEDEMA PERIPHERAL ( 18 FDA reports)
BLOOD UREA INCREASED ( 17 FDA reports)
FACE OEDEMA ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
CONSTIPATION ( 16 FDA reports)
JAUNDICE ( 16 FDA reports)
NEUTROPENIA ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
CARDIAC ARREST ( 15 FDA reports)
GASTRIC ULCER ( 15 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 14 FDA reports)
MULTI-ORGAN FAILURE ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 13 FDA reports)
BLOOD AMYLASE INCREASED ( 13 FDA reports)
INFECTION ( 13 FDA reports)
PALLOR ( 13 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
MUSCULOSKELETAL PAIN ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
ANOREXIA ( 11 FDA reports)
CARDIAC FAILURE CHRONIC ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 10 FDA reports)
CHOLELITHIASIS ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HERPES ZOSTER ( 10 FDA reports)
HYPERURICAEMIA ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
PERITONITIS ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
SWELLING ( 10 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
ATRIAL TACHYCARDIA ( 9 FDA reports)
CARDIAC FAILURE ACUTE ( 9 FDA reports)
ENCEPHALOPATHY ( 9 FDA reports)
EYELID OEDEMA ( 9 FDA reports)
HEART RATE DECREASED ( 9 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
LARGE INTESTINE PERFORATION ( 9 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 9 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
ABDOMINAL PAIN LOWER ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
ANKLE FRACTURE ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BONE ATROPHY ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
FAECES DISCOLOURED ( 8 FDA reports)
GASTRIC NEOPLASM ( 8 FDA reports)
HYPOPHAGIA ( 8 FDA reports)
JOINT SWELLING ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
OCULAR ICTERUS ( 8 FDA reports)
OESOPHAGEAL NEOPLASM ( 8 FDA reports)
PAIN ( 8 FDA reports)
PHARYNGITIS ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
ALOPECIA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD BLISTER ( 7 FDA reports)
CHAPPED LIPS ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
GENITAL EROSION ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
LARGE INTESTINE CARCINOMA ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
MUCOSAL EROSION ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
NIKOLSKY'S SIGN ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
SHOCK HAEMORRHAGIC ( 7 FDA reports)
SKIN EROSION ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
BACTERAEMIA ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PYELONEPHRITIS ( 6 FDA reports)
SERUM FERRITIN INCREASED ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
FALL ( 5 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PROSTATITIS ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DEATH ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
XERODERMA ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BULIMIA NERVOSA ( 3 FDA reports)
CARDIAC AMYLOIDOSIS ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEVICE CONNECTION ISSUE ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTEROCOLITIS VIRAL ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERITONEAL EFFUSION ( 3 FDA reports)
POTTER'S SYNDROME ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
URINE OSMOLARITY INCREASED ( 3 FDA reports)
URINE SODIUM DECREASED ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD ELASTASE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BONE ABSCESS ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMA ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MANIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYELOCYTE COUNT INCREASED ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROBLASTOMA RECURRENT ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERICORONITIS ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SURGERY ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POISONING ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use