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MIGRAINE ( 4 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
RALES ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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