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

NAUSEA ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
CHILLS ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RASH ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
TACHYCARDIA FOETAL ( 3 FDA reports)
TALIPES ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EX-ALCOHOLIC ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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