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
127431751 12743175 1 I 20160829 20160906 20160914 20160914 PER US-JNJFOC-20160907341 JOHNSON AND JOHNSON 69.00 YR E F Y 57.61000 KG 20160914 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
127431751 12743175 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN 19835 10 MG TABLET QD
127431751 12743175 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN 19835 10 MG TABLET QD
127431751 12743175 3 C FLONASE FLUTICASONE PROPIONATE 1 Unknown 0 UNSPECIFIED
127431751 12743175 4 C FLONASE FLUTICASONE PROPIONATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127431751 12743175 1 Cough
127431751 12743175 2 Multiple allergies
127431751 12743175 3 Upper-airway cough syndrome
127431751 12743175 4 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127431751 12743175 Drug ineffective for unapproved indication
127431751 12743175 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
127431751 12743175 1 20160829 0
127431751 12743175 2 20160829 0
127431751 12743175 3 20160826 0
127431751 12743175 4 20160826 0