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
122511172 12251117 2 F 20160325 20160410 20160725 PER US-JNJFOC-20160321746 JANSSEN 71.00 YR E M Y 86.18000 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
122511172 12251117 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN 19835 TABLET
122511172 12251117 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 1 TABLET AT NIGHT, 1 IN MORNING N UNKNOWN 19835 10 MG TABLET BID
122511172 12251117 3 C OTHER THERAPEUTIC PRODUCTS UNSPECIFIED INGREDIENT 1 Unknown 0 UNSPECIFIED
122511172 12251117 4 C OTHER THERAPEUTIC PRODUCTS UNSPECIFIED INGREDIENT 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122511172 12251117 2 Multiple allergies
122511172 12251117 3 Cardiac disorder
122511172 12251117 4 Blood pressure abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122511172 12251117 Drug effect incomplete
122511172 12251117 Overdose
122511172 12251117 Product expiration date issue
122511172 12251117 Product lot number issue
122511172 12251117 Wrong patient received medication

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found