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
127733151 12773315 1 I 20160201 20160922 20160922 PER US-BANPHARM-20164637 BIONPHARMA 0.00 M Y 0.00000 0 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
127733151 12773315 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 1300000724 22429 CAPSULE, SOFT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127733151 12773315 1 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127733151 12773315 Drug ineffective
127733151 12773315 Expired product administered

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found