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

CONVULSION ( 7 FDA reports)
FATIGUE ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
CRYING ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
RASH ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGITATION ( 2 FDA reports)
APHASIA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AURA ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
MANIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL HYPERAEMIA ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)

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