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

FALL ( 9 FDA reports)
FATIGUE ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
RENAL FAILURE ( 5 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BREAST CYST ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
POST PROCEDURAL CONSTIPATION ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
COUGH ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RALES ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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