The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126969751 12696975 1 I 20160801 0 20160829 20160829 DIR 50.00 YR F N 137.00000 LBS 20160826 Y US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126969751 12696975 1 PS BOTOX ONABOTULINUMTOXINA 1 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126969751 12696975 Abdominal discomfort
126969751 12696975 Blood pressure increased
126969751 12696975 Dysphonia
126969751 12696975 Ear pain
126969751 12696975 Eyelid ptosis
126969751 12696975 Headache
126969751 12696975 Malaise
126969751 12696975 Neck pain
126969751 12696975 Vision blurred
126969751 12696975 Visual impairment

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found