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
125889351 12588935 1 I 20160609 20160725 20160725 PER US-JNJFOC-20160615537 JANSSEN 0.00 M Y 0.00000 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
125889351 12588935 1 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 3-4 DAYS N 0 TABLET
125889351 12588935 2 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 3-4 DAYS N 19835 TABLET
125889351 12588935 3 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 3-4 DAYS N 19835 TABLET
125889351 12588935 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 0 UNSPECIFIED
125889351 12588935 5 C FLONASE FLUTICASONE PROPIONATE 1 Unknown 0 UNSPECIFIED
125889351 12588935 6 C FLONASE FLUTICASONE PROPIONATE 1 Unknown 0 UNSPECIFIED
125889351 12588935 7 C FLONASE FLUTICASONE PROPIONATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125889351 12588935 1 Sinus congestion
125889351 12588935 2 Paranasal sinus discomfort
125889351 12588935 3 Multiple allergies
125889351 12588935 4 Thyroid disorder
125889351 12588935 5 Sinus congestion
125889351 12588935 6 Paranasal sinus discomfort
125889351 12588935 7 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125889351 12588935 Drug ineffective for unapproved indication
125889351 12588935 Off label use

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

no results found

Therapies reported

no results found