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DIZZINESS ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CLUMSINESS ( 1 FDA reports)
COMA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
PINEAL NEOPLASM ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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