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

DRUG INTERACTION ( 65 FDA reports)
RENAL FAILURE ACUTE ( 32 FDA reports)
HYPERKALAEMIA ( 23 FDA reports)
FALL ( 22 FDA reports)
PYREXIA ( 22 FDA reports)
DIARRHOEA ( 21 FDA reports)
DIZZINESS ( 20 FDA reports)
SYNCOPE ( 19 FDA reports)
ASTHENIA ( 18 FDA reports)
PULMONARY OEDEMA ( 18 FDA reports)
VOMITING ( 18 FDA reports)
ANAEMIA ( 17 FDA reports)
DYSPNOEA ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
CARDIAC FAILURE ( 16 FDA reports)
HEPATITIS CHOLESTATIC ( 16 FDA reports)
RENAL FAILURE ( 16 FDA reports)
DEATH ( 15 FDA reports)
DISORIENTATION ( 15 FDA reports)
SEPTIC SHOCK ( 14 FDA reports)
THROMBOCYTOPENIA ( 14 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
AMNESIA ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
COORDINATION ABNORMAL ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 9 FDA reports)
APLASIA PURE RED CELL ( 8 FDA reports)
ENTERITIS ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CHOLURIA ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DISCOMFORT ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
PAIN ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TUMOUR INVASION ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECHINOCOCCIASIS ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PIGMENT DISPERSION SYNDROME ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DOLICHOCOLON ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETHROSCOPY ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

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