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
125890881 12589088 1 I 20160623 20160707 20160725 20160725 PER US-JNJFOC-20160707221 JANSSEN 39.09 YR A F Y 0.00000 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
125890881 12589088 1 PS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral U U 999999 50 MG UNSPECIFIED
125890881 12589088 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral U U 19835 UNSPECIFIED
125890881 12589088 3 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral U U 19835 1 DF UNSPECIFIED
125890881 12589088 4 C CLARITIN LORATADINE 1 Unknown 0 1 DF UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125890881 12589088 1 Food allergy
125890881 12589088 3 Food allergy
125890881 12589088 4 Food allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125890881 12589088 Off label use
125890881 12589088 Product use issue
125890881 12589088 Therapeutic response unexpected

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
125890881 12589088 1 20160623 0
125890881 12589088 3 20160623 0