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
125883951 12588395 1 I 20160523 20160725 20160725 PER US-JNJFOC-20160521805 JANSSEN 74.00 YR E F Y 83.92000 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
125883951 12588395 1 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN;464080 0 2 DF TABLET BID
125883951 12588395 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN;464080 0 2 DF TABLET BID
125883951 12588395 3 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN;464080 19835 2 DF TABLET BID
125883951 12588395 4 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN;464080 19835 2 DF TABLET BID
125883951 12588395 5 C PREDNISONE. PREDNISONE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125883951 12588395 1 Urticaria
125883951 12588395 2 Urticaria
125883951 12588395 3 Chronic spontaneous urticaria
125883951 12588395 4 Chronic spontaneous urticaria
125883951 12588395 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125883951 12588395 Off label use
125883951 12588395 Overdose
125883951 12588395 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
125883951 12588395 2 201511 0
125883951 12588395 3 201511 0