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
125883851 12588385 1 I 20160525 20160526 20160725 20160725 PER US-JNJFOC-20160526832 JANSSEN 90.00 YR E F Y 58.97000 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
125883851 12588385 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral U U UNKNOWN;474759 19835 1 DF TABLET
125883851 12588385 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 1 TABLET, ONCE U U UNKNOWN;474759 19835 1 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125883851 12588385 1 Pruritus
125883851 12588385 2 Pruritus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125883851 12588385 Drug ineffective for unapproved indication
125883851 12588385 Off label use
125883851 12588385 Therapeutic response unexpected
125883851 12588385 Wrong patient received medication

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
125883851 12588385 1 20160526 20160526 0
125883851 12588385 2 20160525 20160525 0