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CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
HYPERTENSION ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 15 FDA reports)
MALAISE ( 15 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
ASTHENIA ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
ASTHMA ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
FALL ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
SALIVARY GLAND CANCER ( 5 FDA reports)
SALIVARY GLAND PAIN ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ABASIA ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
COMA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
PAIN ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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