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

DRUG EFFECT DECREASED ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VULVOVAGINAL DISORDER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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