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
126180861 12618086 1 I 20160721 20160721 20160803 20160803 PER US-JNJFOC-20160719985 JANSSEN 50.00 YR A F Y 0.00000 20160803 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
126180861 12618086 1 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y N 0 2 DF TABLET
126180861 12618086 2 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y N 19835 1 DF TABLET
126180861 12618086 3 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y N 19835 1 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126180861 12618086 1 Multiple allergies
126180861 12618086 2 Multiple allergies
126180861 12618086 3 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126180861 12618086 Accidental overdose
126180861 12618086 Dizziness
126180861 12618086 Fatigue

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
126180861 12618086 1 20160721 20160721 0
126180861 12618086 2 20160720 0
126180861 12618086 3 20160722 0