The Safety Rates Drug Report

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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
125883121 12588312 1 I 20160508 20160510 20160725 20160725 PER US-JNJFOC-20160510648 JANSSEN 58.00 YR A F Y 98.88000 KG 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
125883121 12588312 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 19835 10 MG TABLET
125883121 12588312 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 19835 10 MG TABLET
125883121 12588312 3 C POTASSIUM CITRATE. POTASSIUM CITRATE 1 Unknown 0 UNKNOWN
125883121 12588312 4 C FLONASE FLUTICASONE PROPIONATE 1 Unknown 0 SPRAY
125883121 12588312 5 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Unknown 6 WEEKS 0 SPRAY
125883121 12588312 6 C LOSARTAN. LOSARTAN 1 Unknown 100MG/12.5 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125883121 12588312 1 Multiple allergies
125883121 12588312 2 Multiple allergies
125883121 12588312 3 Dyspepsia
125883121 12588312 4 Hypersensitivity
125883121 12588312 5 Asthma
125883121 12588312 6 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125883121 12588312 Rash
125883121 12588312 Urticaria

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

no results found

Therapies reported

no results found