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
125882861 12588286 1 I 20160509 20160510 20160725 20160725 PER US-JNJFOC-20160510500 JANSSEN 69.00 YR E F Y 48.08000 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
125882861 12588286 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y N 471994 19835 1 DF TABLET
125882861 12588286 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y N 471994 19835 1 DF TABLET
125882861 12588286 3 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown INTERVAL: YEARS 0 50 MG UNSPECIFIED
125882861 12588286 4 C PRAVASTATIN. PRAVASTATIN 1 Unknown INTERVAL: YEARS 0 20 MG UNSPECIFIED
125882861 12588286 5 C WARFARIN WARFARIN 1 Unknown 3MG/4.5MG, INTERVAL: YEARS 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125882861 12588286 1 Swelling face
125882861 12588286 2 Multiple allergies
125882861 12588286 3 Thyroid disorder
125882861 12588286 4 Blood cholesterol abnormal
125882861 12588286 5 Anticoagulant therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125882861 12588286 Feeling abnormal
125882861 12588286 Headache

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
125882861 12588286 1 20160509 20160509 0
125882861 12588286 2 20160509 20160509 0