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

HEADACHE ( 14 FDA reports)
ARTHRALGIA ( 12 FDA reports)
COORDINATION ABNORMAL ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
ADVERSE EVENT ( 9 FDA reports)
AGITATION ( 9 FDA reports)
APATHY ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
CHILLS ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
CRYING ( 9 FDA reports)
DEPERSONALISATION ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
DYSPHORIA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
EAR INFECTION ( 9 FDA reports)
EMOTIONAL DISORDER ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
HEAD DISCOMFORT ( 9 FDA reports)
HYPERAESTHESIA ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
MALAISE ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
MYDRIASIS ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
NERVOUSNESS ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PHOTOSENSITIVITY REACTION ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
SENSATION OF HEAVINESS ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SLEEP DISORDER ( 9 FDA reports)
SOCIAL PROBLEM ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
TREMOR ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
WITHDRAWAL SYNDROME ( 9 FDA reports)
EAR PAIN ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
POISONING ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
STRESS ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
BURNING SENSATION ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
PAIN ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CONGENITAL ECTOPIC PANCREAS ( 3 FDA reports)
DETOXIFICATION ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ARTERIAL SPASM ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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