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

ABNORMAL BEHAVIOUR ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
SOMNAMBULISM ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
DELUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
TREMOR ( 2 FDA reports)
STRESS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CRYING ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FACE INJURY ( 1 FDA reports)
FALL ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
MANIA ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SNORING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)

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