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
123680032 12368003 2 F 20160420 20160513 20160725 PER US-JNJFOC-20160421238 JANSSEN 60.00 YR A F Y 65.77000 KG 20160725 CN US 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
123680032 12368003 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral START: AT ABOUT 1700 HOURS U U UNKNOWN 19835 1 DF TABLET
123680032 12368003 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral START: AT ABOUT 1700 HOURS U U UNKNOWN 19835 1 DF TABLET
123680032 12368003 3 C CORTISONE CORTISONEHYDROCORTISONE 1 Unknown 0 UNSPECIFIED
123680032 12368003 4 C CORTISONE CORTISONEHYDROCORTISONE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123680032 12368003 1 Hypersensitivity
123680032 12368003 2 Urticaria
123680032 12368003 3 Hypersensitivity
123680032 12368003 4 Urticaria

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123680032 12368003 Off label use
123680032 12368003 Product use issue

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
123680032 12368003 1 20160419 0
123680032 12368003 2 20160419 0