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
127021551 12702155 1 I 201608 20160817 20160831 20160831 PER US-JNJFOC-20160815619 JOHNSON AND JOHNSON 94.94 YR E F Y 43.09000 KG 20160831 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
127021551 12702155 1 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y U 0 10 MG TABLET
127021551 12702155 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y U 0 5 MG TABLET
127021551 12702155 3 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y U 19835 10 MG TABLET
127021551 12702155 4 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral Y U 19835 5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127021551 12702155 1 Dry skin
127021551 12702155 2 Dry skin
127021551 12702155 3 Pruritus
127021551 12702155 4 Pruritus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127021551 12702155 Fatigue
127021551 12702155 Off label use
127021551 12702155 Somnolence
127021551 12702155 Therapeutic response unexpected

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
127021551 12702155 1 20160815 0
127021551 12702155 2 20160816 0
127021551 12702155 3 20160815 0
127021551 12702155 4 20160816 0