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
125890671 12589067 1 I 20160624 20160701 20160725 20160725 PER US-JNJFOC-20160702644 JANSSEN 72.00 YR E M Y 72.58000 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
125890671 12589067 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 10 MG N 475920 19835 1 DF TABLET
125890671 12589067 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 10 MG N 475920 19835 1 DF TABLET
125890671 12589067 3 C ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Unknown 1 EVERY OTHER FOR YEARS 0 10 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125890671 12589067 1 Rhinorrhoea
125890671 12589067 2 Eye pruritus
125890671 12589067 3 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125890671 12589067 Drug administration error
125890671 12589067 Rash erythematous

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
125890671 12589067 1 20160624 0
125890671 12589067 2 20160624 0