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

SCHIZOPHRENIA ( 8 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
WATER INTOXICATION ( 5 FDA reports)
FALL ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VOMITING ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
TETANY ( 2 FDA reports)
SNORING ( 2 FDA reports)
CAFFEINE CONSUMPTION ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
HYPOTENSION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)

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