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

WEIGHT INCREASED ( 4 FDA reports)
ANGER ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACNE ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATITIS B ANTIBODY ABNORMAL ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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