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

PAIN ( 47 FDA reports)
HEADACHE ( 33 FDA reports)
PNEUMONIA ( 33 FDA reports)
BREAST MASS ( 32 FDA reports)
HYPERGLYCAEMIA ( 32 FDA reports)
DYSPNOEA ( 23 FDA reports)
BLOOD PRESSURE INCREASED ( 22 FDA reports)
LUNG DISORDER ( 16 FDA reports)
CARDIOMEGALY ( 15 FDA reports)
HYPOTENSION ( 15 FDA reports)
PERICARDIAL EFFUSION ( 15 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
PERIARTHRITIS ( 14 FDA reports)
VOMITING ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
BRAIN SCAN ABNORMAL ( 11 FDA reports)
FLUID RETENTION ( 11 FDA reports)
HEPATIC NEOPLASM ( 11 FDA reports)
LIVER OPERATION ( 11 FDA reports)
MENINGIOMA ( 11 FDA reports)
NERVOUSNESS ( 11 FDA reports)
ROAD TRAFFIC ACCIDENT ( 11 FDA reports)
ASPIRATION ( 10 FDA reports)
FACIAL PARESIS ( 10 FDA reports)
HEMIPARESIS ( 10 FDA reports)
HIGH FREQUENCY ABLATION ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
LETHARGY ( 10 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 10 FDA reports)
METASTASES TO SPINE ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
POST PROCEDURAL COMPLICATION ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
SURGERY ( 10 FDA reports)
UNRESPONSIVE TO STIMULI ( 10 FDA reports)
BRAIN NEOPLASM ( 9 FDA reports)
INJECTION SITE SWELLING ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
DEATH ( 6 FDA reports)
DIVERTICULAR PERFORATION ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
FALL ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
KIDNEY INFECTION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LENTIGO ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NODULE ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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