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

DRUG INTERACTION ( 5 FDA reports)
ABASIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STARING ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENSION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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