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
125883771 12588377 1 I 20160525 20160526 20160725 20160725 PER US-JNJFOC-20160526891 JANSSEN 75.00 YR E F Y 95.26000 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
125883771 12588377 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 464069 19835 TABLET
125883771 12588377 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 464069 19835 10 MG TABLET QD
125883771 12588377 3 C VITAMIN B12 CYANOCOBALAMIN 1 Unknown 0 5000 MG UNSPECIFIED
125883771 12588377 4 C VITAMIN D3 CHOLECALCIFEROL 1 Unknown 0 1 DF UNSPECIFIED
125883771 12588377 5 C FUROSEMIDE. FUROSEMIDE 1 Unknown 0 1 DF UNSPECIFIED
125883771 12588377 6 C CALCIUM CALCIUM 1 Unknown 0 2 DF UNSPECIFIED
125883771 12588377 7 C ZANTAC RANITIDINE HYDROCHLORIDE 1 Unknown 0 2 DF UNSPECIFIED
125883771 12588377 8 C ASPIRIN. ASPIRIN 1 Unknown 0 1 DF UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125883771 12588377 2 Multiple allergies
125883771 12588377 3 Routine health maintenance
125883771 12588377 4 Routine health maintenance
125883771 12588377 5 Fluid retention
125883771 12588377 6 Supplementation therapy
125883771 12588377 7 Ulcer
125883771 12588377 8 Cardiac disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125883771 12588377 Fatigue
125883771 12588377 Somnolence

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
125883771 12588377 2 20160525 0