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

PAIN IN EXTREMITY ( 12 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
DIARRHOEA ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
MYOCLONUS ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
ABDOMINAL NEOPLASM ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DROP ATTACKS ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
GINGIVAL DISORDER ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
ORAL DISCOMFORT ( 5 FDA reports)
SALIVA ALTERED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHILLS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYST ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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