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
126180881 12618088 1 I 20160722 20160722 20160803 20160803 PER US-JNJFOC-20160720093 JANSSEN 66.00 YR E F Y 54.43000 KG 20160803 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
126180881 12618088 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N N 467844 19835 TABLET
126180881 12618088 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N N 467844 19835 10 MG TABLET QD
126180881 12618088 3 C ATORVASTATIN ATORVASTATIN 1 Unknown FOR 26 YEARS 0 20 MG UNSPECIFIED
126180881 12618088 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown FOR 3 WEEKS 0 5 MG UNSPECIFIED
126180881 12618088 5 C LISINOPRIL. LISINOPRIL 1 Unknown FOR 26 YEARS 0 40 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126180881 12618088 2 Multiple allergies
126180881 12618088 3 Blood cholesterol increased
126180881 12618088 4 Hypertension
126180881 12618088 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126180881 12618088 Chest pain

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
126180881 12618088 2 20160721 0