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
123677982 12367798 2 F 20160406 20160411 20160513 20160725 PER US-JNJFOC-20160408175 JANSSEN 58.00 YR A F Y 57.61000 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
123677982 12367798 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N N 426865 19835 TABLET
123677982 12367798 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N N 426865 19835 10 MG TABLET
123677982 12367798 3 C OMEGA 3 OMEGA-3 FATTY ACIDS 1 Unknown 0 CAPSULE
123677982 12367798 4 C VITAMIN C ASCORBIC ACID 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123677982 12367798 2 Seasonal allergy
123677982 12367798 3 Nutritional supplementation
123677982 12367798 4 Nutritional supplementation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123677982 12367798 Chapped lips
123677982 12367798 Drug ineffective
123677982 12367798 Headache
123677982 12367798 Insomnia
123677982 12367798 Oral mucosal blistering
123677982 12367798 Product outer packaging issue

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
123677982 12367798 2 20160406 20160406 0