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
126931391 12693139 1 I 20160815 0 20160826 20160826 DIR 50.00 YR N 93.00000 LBS 20160825 N 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
126931391 12693139 1 PS BOTOX ONABOTULINUMTOXINA 1 N D 0
126931391 12693139 3 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 0
126931391 12693139 5 C CLONIDINE. CLONIDINE 1 0
126931391 12693139 7 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126931391 12693139 1 Migraine prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126931391 12693139 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126931391 12693139 Dysphagia
126931391 12693139 Headache
126931391 12693139 Nausea
126931391 12693139 Neck pain

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126931391 12693139 1 20160810 0