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

FATIGUE ( 27 FDA reports)
NAUSEA ( 27 FDA reports)
DIZZINESS ( 26 FDA reports)
HEADACHE ( 26 FDA reports)
NEUROPATHY PERIPHERAL ( 26 FDA reports)
BLOOD CALCIUM DECREASED ( 25 FDA reports)
BLOOD CREATININE INCREASED ( 25 FDA reports)
BLOOD UREA INCREASED ( 25 FDA reports)
CONFUSIONAL STATE ( 25 FDA reports)
COORDINATION ABNORMAL ( 25 FDA reports)
COUGH ( 25 FDA reports)
DEEP VEIN THROMBOSIS ( 25 FDA reports)
DYSPNOEA ( 25 FDA reports)
ERYTHEMA ( 25 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 25 FDA reports)
FISTULA ( 25 FDA reports)
GINGIVAL ULCERATION ( 25 FDA reports)
GINGIVITIS ( 25 FDA reports)
HYPERCALCAEMIA ( 25 FDA reports)
IMPAIRED HEALING ( 25 FDA reports)
MUSCLE SPASMS ( 25 FDA reports)
MUSCULAR WEAKNESS ( 25 FDA reports)
OSTEOMYELITIS ( 25 FDA reports)
PAIN ( 25 FDA reports)
PAIN IN EXTREMITY ( 25 FDA reports)
PLEURAL EFFUSION ( 25 FDA reports)
PRIMARY SEQUESTRUM ( 25 FDA reports)
RASH ( 25 FDA reports)
RHINITIS ( 25 FDA reports)
TOOTH DISORDER ( 25 FDA reports)
CARDIOMYOPATHY ( 24 FDA reports)
MENTAL STATUS CHANGES ( 24 FDA reports)
MASTICATION DISORDER ( 23 FDA reports)
TOOTHACHE ( 21 FDA reports)
VISUAL IMPAIRMENT ( 21 FDA reports)
ANAEMIA ( 20 FDA reports)
MITRAL VALVE INCOMPETENCE ( 20 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 20 FDA reports)
BACK PAIN ( 19 FDA reports)
BONE DISORDER ( 19 FDA reports)
DEHYDRATION ( 19 FDA reports)
DYSPHEMIA ( 19 FDA reports)
MEMORY IMPAIRMENT ( 19 FDA reports)
MUSCLE TWITCHING ( 19 FDA reports)
PHARYNGEAL OEDEMA ( 19 FDA reports)
SLEEP APNOEA SYNDROME ( 19 FDA reports)
WEIGHT INCREASED ( 19 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 18 FDA reports)
DYSURIA ( 18 FDA reports)
INSOMNIA ( 18 FDA reports)
LOBAR PNEUMONIA ( 18 FDA reports)
PANCYTOPENIA ( 18 FDA reports)
PLEURITIC PAIN ( 18 FDA reports)
POLYURIA ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
RESTLESS LEGS SYNDROME ( 18 FDA reports)
RHONCHI ( 18 FDA reports)
STRESS ( 18 FDA reports)
TELANGIECTASIA ( 18 FDA reports)
ANEURYSM ( 17 FDA reports)
DEAFNESS NEUROSENSORY ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
BONE DEBRIDEMENT ( 16 FDA reports)
CARPAL TUNNEL SYNDROME ( 16 FDA reports)
CATHETER REMOVAL ( 16 FDA reports)
CELLULITIS ( 16 FDA reports)
CEREBROVASCULAR ACCIDENT ( 16 FDA reports)
DIABETES MELLITUS ( 16 FDA reports)
DROP ATTACKS ( 16 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 16 FDA reports)
HYPERLIPIDAEMIA ( 16 FDA reports)
HYPERTENSION ( 16 FDA reports)
INCISIONAL DRAINAGE ( 16 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 16 FDA reports)
LOOSE TOOTH ( 16 FDA reports)
ORAL SURGERY ( 16 FDA reports)
OSTEOARTHRITIS ( 16 FDA reports)
SWELLING ( 16 FDA reports)
SYNCOPE ( 16 FDA reports)
THYROID NEOPLASM ( 16 FDA reports)
TOOTH ABSCESS ( 16 FDA reports)
TOOTH EXTRACTION ( 16 FDA reports)
AORTIC ANEURYSM ( 15 FDA reports)
ARTHRITIS ( 15 FDA reports)
DEPRESSION ( 15 FDA reports)
DEVICE OCCLUSION ( 15 FDA reports)
HIATUS HERNIA ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
VOMITING ( 15 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 13 FDA reports)
OSTEONECROSIS OF JAW ( 13 FDA reports)
JAW OPERATION ( 12 FDA reports)
OSTEONECROSIS ( 12 FDA reports)
BONE DENSITY DECREASED ( 10 FDA reports)
CAROTID ARTERY DISEASE ( 10 FDA reports)
CEREBRAL ISCHAEMIA ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
DIVERTICULUM ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
SWELLING FACE ( 10 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
DENTAL CARE ( 9 FDA reports)
EXOSTOSIS ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
MORTON'S NEUROMA ( 9 FDA reports)
NEOPLASM MALIGNANT ( 9 FDA reports)
PERIARTHRITIS ( 9 FDA reports)
PLANTAR FASCIITIS ( 9 FDA reports)
CORONARY ARTERY BYPASS ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
ATELECTASIS ( 7 FDA reports)
BONE LOSS ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
EXPOSED BONE IN JAW ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 5 FDA reports)
DENTAL TREATMENT ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
OVARIAN EPITHELIAL CANCER ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ANAL FISSURE ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
SCAR ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MASS ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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