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

ARTHRALGIA ( 7 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
KYPHOSIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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