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

CONVULSION ( 8 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
PAIN ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
AURA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
EPILEPTIC AURA ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THIRST ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
CANDIDIASIS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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