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

DEPRESSION ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
FATIGUE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
PAIN ( 3 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FALL ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMPLANT SITE PRURITUS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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