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
126180671 12618067 1 I 20160712 20160713 20160803 20160803 PER US-JNJFOC-20160711895 JANSSEN 84.00 YR E M Y 86.18000 KG 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
126180671 12618067 1 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 1 TABLET N 476029 0 10 MG TABLET QD
126180671 12618067 2 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 1 TABLET N 476029 19835 10 MG TABLET QD
126180671 12618067 3 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 1 TABLET N 476029 19835 10 MG TABLET QD
126180671 12618067 4 C ASPIRIN. ASPIRIN 1 Unknown DAILY 0 81 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126180671 12618067 1 Lacrimation increased
126180671 12618067 2 Eye swelling
126180671 12618067 3 Multiple allergies
126180671 12618067 4 Cardiac disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126180671 12618067 Drug administration error
126180671 12618067 Drug ineffective for unapproved indication
126180671 12618067 Off label use

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
126180671 12618067 1 20160712 0
126180671 12618067 2 20160712 0
126180671 12618067 3 20160712 0