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
125883831 12588383 1 I 20160602 20160603 20160725 20160725 PER US-JNJFOC-20160604474 JANSSEN 82.00 YR E M Y 76.20000 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
125883831 12588383 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown N 464068 19835 TABLET
125883831 12588383 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown N 464068 19835 10 MG TABLET QD
125883831 12588383 3 C TOPROL XL METOPROLOL SUCCINATE 1 Unknown 0 UNSPECIFIED
125883831 12588383 4 C FELODIPINE. FELODIPINE 1 Unknown 0 UNSPECIFIED
125883831 12588383 5 C ASPIRIN. ASPIRIN 1 Unknown 0 UNSPECIFIED
125883831 12588383 6 C LIPITOR ATORVASTATIN CALCIUM 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125883831 12588383 2 Rash
125883831 12588383 3 Blood pressure measurement
125883831 12588383 4 Blood pressure measurement
125883831 12588383 5 Blood pressure measurement
125883831 12588383 6 Blood cholesterol abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125883831 12588383 Abdominal pain upper
125883831 12588383 Off label use
125883831 12588383 Product packaging issue
125883831 12588383 Product use issue

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
125883831 12588383 2 20160602 0