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

FATIGUE ( 62 FDA reports)
NAUSEA ( 57 FDA reports)
HYPOTENSION ( 49 FDA reports)
PYREXIA ( 47 FDA reports)
ASTHENIA ( 46 FDA reports)
DIARRHOEA ( 43 FDA reports)
BLOOD BILIRUBIN INCREASED ( 35 FDA reports)
CONFUSIONAL STATE ( 34 FDA reports)
DIZZINESS ( 32 FDA reports)
VOMITING ( 30 FDA reports)
CHILLS ( 28 FDA reports)
DEPRESSION ( 27 FDA reports)
HEADACHE ( 27 FDA reports)
PAIN ( 27 FDA reports)
DYSPNOEA ( 26 FDA reports)
ABDOMINAL PAIN ( 24 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 24 FDA reports)
ANXIETY ( 24 FDA reports)
OEDEMA PERIPHERAL ( 24 FDA reports)
PAIN IN EXTREMITY ( 24 FDA reports)
THROMBOCYTOPENIA ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
HYPOAESTHESIA ( 23 FDA reports)
PLEURAL EFFUSION ( 23 FDA reports)
ANAEMIA ( 22 FDA reports)
CHEST PAIN ( 21 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
PRURITUS ( 21 FDA reports)
DEHYDRATION ( 20 FDA reports)
GRAFT VERSUS HOST DISEASE ( 20 FDA reports)
HYPERTENSION ( 20 FDA reports)
JAUNDICE ( 19 FDA reports)
MULTI-ORGAN FAILURE ( 19 FDA reports)
MUSCULAR WEAKNESS ( 19 FDA reports)
RESPIRATORY FAILURE ( 19 FDA reports)
SEPSIS ( 19 FDA reports)
SOMNOLENCE ( 19 FDA reports)
ASCITES ( 18 FDA reports)
RENAL FAILURE ( 18 FDA reports)
BACK PAIN ( 17 FDA reports)
RASH ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
CHOLELITHIASIS ( 16 FDA reports)
URINARY TRACT INFECTION ( 16 FDA reports)
ARTHRALGIA ( 15 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 15 FDA reports)
DEATH ( 15 FDA reports)
DECREASED APPETITE ( 15 FDA reports)
HEART RATE INCREASED ( 15 FDA reports)
HEPATIC FAILURE ( 15 FDA reports)
HEPATITIS ( 15 FDA reports)
MENTAL STATUS CHANGES ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
CHROMATURIA ( 14 FDA reports)
HEPATIC ENZYME INCREASED ( 14 FDA reports)
HOT FLUSH ( 14 FDA reports)
INSOMNIA ( 14 FDA reports)
LIVER ABSCESS ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
PARAESTHESIA ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
COUGH ( 13 FDA reports)
FALL ( 13 FDA reports)
TREMOR ( 13 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
BONE PAIN ( 12 FDA reports)
CHOLANGITIS ( 12 FDA reports)
COAGULOPATHY ( 12 FDA reports)
ENTEROCOCCAL INFECTION ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
LIVER TRANSPLANT REJECTION ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
SPLENOMEGALY ( 12 FDA reports)
AMNESIA ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
BLOOD UREA INCREASED ( 11 FDA reports)
CHOLESTASIS ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
DEFORMITY ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
HEPATOTOXICITY ( 11 FDA reports)
INJURY ( 11 FDA reports)
LEUKOCYTOSIS ( 11 FDA reports)
MALAISE ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
CONVULSION ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
GALLBLADDER DISORDER ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
RENAL FAILURE CHRONIC ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ANASTOMOTIC STENOSIS ( 9 FDA reports)
ATELECTASIS ( 9 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
ATRIAL FLUTTER ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
METRORRHAGIA ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
PROCEDURAL PAIN ( 9 FDA reports)
PRODUCT QUALITY ISSUE ( 9 FDA reports)
STRESS ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DISEASE RECURRENCE ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
GENERALISED OEDEMA ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPOVOLAEMIA ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
THYROID NEOPLASM ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 7 FDA reports)
DILATATION VENTRICULAR ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
FEELING COLD ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
GALLBLADDER OEDEMA ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
THIRST ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
ABSCESS DRAINAGE ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
BREAST ABSCESS ( 6 FDA reports)
BREAST CELLULITIS ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
CHOLANGIOGRAM ( 6 FDA reports)
CHOLANGITIS SCLEROSING ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
GALACTORRHOEA ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HEPATIC CYST ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HEPATIC VEIN STENOSIS ( 6 FDA reports)
ILEUS ( 6 FDA reports)
INTERNAL HERNIA ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
MENTAL IMPAIRMENT ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
NEURITIS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SKIN HYPERPIGMENTATION ( 6 FDA reports)
SKIN HYPERTROPHY ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 5 FDA reports)
AGITATION ( 5 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 5 FDA reports)
AORTIC VALVE STENOSIS ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
BREAST CANCER FEMALE ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CAROTID ARTERY STENOSIS ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
COLONIC POLYP ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HEPATIC ARTERY OCCLUSION ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PERIRECTAL ABSCESS ( 5 FDA reports)
PERITONITIS BACTERIAL ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PLEURITIC PAIN ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
SWELLING ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ADENOCARCINOMA PANCREAS ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SCAR ( 4 FDA reports)
SKIN FIBROSIS ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BILE DUCT NECROSIS ( 3 FDA reports)
BILIARY CIRRHOSIS ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
COELIAC ARTERY STENOSIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DUODENOGASTRIC REFLUX ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
FAECAL VOLUME DECREASED ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HAEMOSIDEROSIS ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PEAU D'ORANGE ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
SPLENIC LESION ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
THALASSAEMIA ALPHA ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VIIITH NERVE LESION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS JAW ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC VALVE ATRESIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLESTASIS OF PREGNANCY ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
COARCTATION OF THE AORTA ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MACROCEPHALY ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OPHTHALMOLOGICAL EXAMINATION NORMAL ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPLENIC INFECTION ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATELECTASIS NEONATAL ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE OUTPUT DECREASED ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
COAGULATION DISORDER NEONATAL ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL OPERATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEUKAEMIC INFILTRATION ( 1 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRECIPITATE LABOUR ( 1 FDA reports)
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PROSTATIC DISORDER ( 1 FDA reports)
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PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
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PRURITUS GENERALISED ( 1 FDA reports)
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PSORIASIS ( 1 FDA reports)
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PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
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PYLORIC STENOSIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
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RASH SCALY ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
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RHEUMATOID ARTHRITIS ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
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SHOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
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SLEEP WALKING ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SPINAL CORD OPERATION ( 1 FDA reports)
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STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
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SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
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THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
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TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
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ULCER ( 1 FDA reports)
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