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

DIARRHOEA ( 61 FDA reports)
NAUSEA ( 58 FDA reports)
VOMITING ( 58 FDA reports)
DYSPNOEA ( 54 FDA reports)
ANAEMIA ( 51 FDA reports)
RENAL FAILURE ACUTE ( 51 FDA reports)
HYPERTENSION ( 44 FDA reports)
PAIN ( 41 FDA reports)
RENAL FAILURE ( 39 FDA reports)
URINARY TRACT INFECTION ( 38 FDA reports)
ABDOMINAL PAIN ( 35 FDA reports)
ASTHENIA ( 35 FDA reports)
HAEMOGLOBIN DECREASED ( 35 FDA reports)
HEADACHE ( 35 FDA reports)
OEDEMA PERIPHERAL ( 35 FDA reports)
FALL ( 33 FDA reports)
PYREXIA ( 33 FDA reports)
DIZZINESS ( 31 FDA reports)
ANXIETY ( 30 FDA reports)
DEHYDRATION ( 30 FDA reports)
PLEURAL EFFUSION ( 30 FDA reports)
DRUG INTERACTION ( 29 FDA reports)
MALAISE ( 29 FDA reports)
ARTHRALGIA ( 26 FDA reports)
HYPOKALAEMIA ( 26 FDA reports)
CELLULITIS ( 25 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 25 FDA reports)
INJURY ( 25 FDA reports)
LEUKOPENIA ( 25 FDA reports)
PRURITUS ( 25 FDA reports)
BLOOD CREATININE INCREASED ( 24 FDA reports)
INFECTION ( 24 FDA reports)
EMOTIONAL DISTRESS ( 23 FDA reports)
HYPERKALAEMIA ( 23 FDA reports)
HYPOTENSION ( 23 FDA reports)
THROMBOCYTOPENIA ( 23 FDA reports)
ATELECTASIS ( 22 FDA reports)
MALNUTRITION ( 22 FDA reports)
BRONCHOPNEUMONIA ( 21 FDA reports)
CONFUSIONAL STATE ( 21 FDA reports)
CONTUSION ( 21 FDA reports)
FATIGUE ( 21 FDA reports)
GAIT DISTURBANCE ( 21 FDA reports)
HAEMATURIA ( 21 FDA reports)
SCAR ( 21 FDA reports)
WEIGHT DECREASED ( 21 FDA reports)
NEUTROPENIA ( 20 FDA reports)
BACK PAIN ( 19 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 19 FDA reports)
COLLAPSE OF LUNG ( 19 FDA reports)
HYPONATRAEMIA ( 19 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 19 FDA reports)
METASTASES TO BONE ( 19 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 18 FDA reports)
DEPRESSION ( 18 FDA reports)
LYMPHADENOPATHY ( 18 FDA reports)
PANCYTOPENIA ( 18 FDA reports)
PHYSICAL DISABILITY ( 18 FDA reports)
RASH ( 18 FDA reports)
SOMNOLENCE ( 18 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 17 FDA reports)
MENTAL STATUS CHANGES ( 17 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
OSTEOPENIA ( 16 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 15 FDA reports)
METASTASES TO LIVER ( 15 FDA reports)
METASTASES TO SPINE ( 15 FDA reports)
METASTASES TO THORAX ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
STRESS FRACTURE ( 15 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BONE LESION ( 14 FDA reports)
BONE MARROW OEDEMA ( 14 FDA reports)
CARCINOID SYNDROME ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
EFFUSION ( 14 FDA reports)
ENTHESOPATHY ( 14 FDA reports)
FOOT FRACTURE ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPOPHOSPHATAEMIA ( 14 FDA reports)
INTESTINAL RESECTION ( 14 FDA reports)
METABOLIC ACIDOSIS ( 14 FDA reports)
OSTEONECROSIS OF JAW ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
PLANTAR FASCIITIS ( 14 FDA reports)
SYNOVIAL CYST ( 14 FDA reports)
TENDON DISORDER ( 14 FDA reports)
TRAUMATIC HAEMATOMA ( 14 FDA reports)
VISUAL IMPAIRMENT ( 14 FDA reports)
BONE PAIN ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
DEATH ( 13 FDA reports)
DYSPEPSIA ( 13 FDA reports)
FLUSHING ( 13 FDA reports)
HYPOMAGNESAEMIA ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
OSTEOSCLEROSIS ( 13 FDA reports)
PULMONARY GRANULOMA ( 13 FDA reports)
SYNCOPE ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
ABSCESS LIMB ( 12 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
COUGH ( 12 FDA reports)
DRY MOUTH ( 12 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 12 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 12 FDA reports)
LUNG CONSOLIDATION ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
SCOLIOSIS ( 12 FDA reports)
TREMOR ( 12 FDA reports)
VENTRICULAR TACHYCARDIA ( 12 FDA reports)
ASCITES ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
CHILLS ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
HEPATIC ENCEPHALOPATHY ( 11 FDA reports)
INFLAMMATION ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
WOUND COMPLICATION ( 11 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BURSITIS ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 10 FDA reports)
HYPOCALCAEMIA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
SLEEP APNOEA SYNDROME ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
FLUID RETENTION ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
HEPATIC LESION ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
HYPERURICAEMIA ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
MALABSORPTION ( 9 FDA reports)
NEUROENDOCRINE TUMOUR ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 9 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 8 FDA reports)
ARTHRITIS ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HAEMORRHOIDS ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
HYPERCHLORAEMIA ( 8 FDA reports)
HYPOALBUMINAEMIA ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
VENOUS THROMBOSIS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
BLINDNESS ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 7 FDA reports)
METASTATIC CARCINOID TUMOUR ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
NEUTROPENIC COLITIS ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
AGITATION ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
DRUG DISPENSING ERROR ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
GOUT ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
PERITONITIS BACTERIAL ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 6 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
APPLICATION SITE PAIN ( 5 FDA reports)
APPLICATION SITE PRURITUS ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DRUG EFFECT INCREASED ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
RENAL PAIN ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACIDOSIS ( 4 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BLADDER PAIN ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SPINAL LAMINECTOMY ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ANGER ( 3 FDA reports)
APHONIA ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CYSTITIS RADIATION ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NODULE ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PNEUMATOSIS INTESTINALIS ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SMOKER ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COMA ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CRYING ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EXTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HERNIAL EVENTRATION ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RALES ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
ULCER ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORONA VIRUS INFECTION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHLORURIA ( 1 FDA reports)
HYPERMAGNESURIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEAD DISLODGEMENT ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL INFECTION ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DYSTROPHY ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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