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TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
HYPERTENSION ( 6 FDA reports)
HEADACHE ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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