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

PAIN ( 18 FDA reports)
ANAEMIA ( 17 FDA reports)
NAUSEA ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
DEPRESSION ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
HYPOALBUMINAEMIA ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
DEEP VEIN THROMBOSIS ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
BONE DISORDER ( 11 FDA reports)
CHOLECYSTITIS ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
FALL ( 11 FDA reports)
INFECTION ( 11 FDA reports)
RENAL FAILURE ( 11 FDA reports)
ABDOMINAL HERNIA ( 10 FDA reports)
ARTERIOSCLEROSIS ( 10 FDA reports)
BACK PAIN ( 10 FDA reports)
BACTERIAL INFECTION ( 10 FDA reports)
BEDRIDDEN ( 10 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 10 FDA reports)
BLINDNESS ( 10 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 10 FDA reports)
BONE LESION ( 10 FDA reports)
BONE PAIN ( 10 FDA reports)
BONE SCAN ABNORMAL ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 10 FDA reports)
CHRONIC SINUSITIS ( 10 FDA reports)
COLONIC POLYP ( 10 FDA reports)
COMPRESSION FRACTURE ( 10 FDA reports)
CYST ( 10 FDA reports)
CYSTITIS ( 10 FDA reports)
DIVERTICULUM ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
EPISTAXIS ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
FISTULA ( 10 FDA reports)
GASTRIC DISORDER ( 10 FDA reports)
GINGIVAL DISORDER ( 10 FDA reports)
GOITRE ( 10 FDA reports)
GYNAECOMASTIA ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
HYPERCHOLESTEROLAEMIA ( 10 FDA reports)
HYPERPARATHYROIDISM ( 10 FDA reports)
HYPOAESTHESIA ORAL ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
IRRITABLE BOWEL SYNDROME ( 10 FDA reports)
JAW DISORDER ( 10 FDA reports)
JAW FRACTURE ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
MANIA ( 10 FDA reports)
MELANOCYTIC NAEVUS ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
NEUTROPENIA ( 10 FDA reports)
NOCTURIA ( 10 FDA reports)
OBSTRUCTIVE UROPATHY ( 10 FDA reports)
OCCULT BLOOD POSITIVE ( 10 FDA reports)
ONYCHOMYCOSIS ( 10 FDA reports)
ORAL DISCHARGE ( 10 FDA reports)
OROPHARYNGEAL PAIN ( 10 FDA reports)
OSTEITIS ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
OSTEOPENIA ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PARATHYROID TUMOUR BENIGN ( 10 FDA reports)
PULMONARY GRANULOMA ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
RENAL CYST ( 10 FDA reports)
RENAL FAILURE CHRONIC ( 10 FDA reports)
RETINAL ISCHAEMIA ( 10 FDA reports)
RIB FRACTURE ( 10 FDA reports)
SLEEP APNOEA SYNDROME ( 10 FDA reports)
SPINAL OSTEOARTHRITIS ( 10 FDA reports)
SWELLING FACE ( 10 FDA reports)
THYROID CANCER ( 10 FDA reports)
TOOTH ABSCESS ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
URINE OUTPUT ( 10 FDA reports)
DIZZINESS ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
HYPERLIPIDAEMIA ( 9 FDA reports)
KYPHOSIS ( 9 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
ANXIETY ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
GASTRODUODENITIS ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
OSTEONECROSIS OF JAW ( 8 FDA reports)
ANIMAL BITE ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
NIGHT SWEATS ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 7 FDA reports)
FEAR ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ATAXIA ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ABSCESS DRAINAGE ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
BENIGN TUMOUR EXCISION ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BONE DEBRIDEMENT ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIP PAIN ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PENILE PROSTHESIS INSERTION ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJURY ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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