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
125889592 12588959 2 F 20160726 20160725 20160803 PER US-JNJFOC-20160616857 JANSSEN 0.00 M Y 0.00000 20160803 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
125889592 12588959 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown U U UNKNOWN 19835 UNSPECIFIED
125889592 12588959 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown U U UNKNOWN 19835 UNSPECIFIED
125889592 12588959 3 C MUCINEX GUAIFENESIN 1 Unknown 12 MONTHS 0 UNSPECIFIED
125889592 12588959 4 C XTANDI ENZALUTAMIDE 1 Unknown 3 CAPSULES DAILY (120 MG) 0 40 MG CAPSULE TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125889592 12588959 1 Hypersensitivity
125889592 12588959 2 Mucous membrane disorder
125889592 12588959 3 Mucous membrane disorder
125889592 12588959 4 Prostatic specific antigen

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125889592 12588959 Drug ineffective
125889592 12588959 Drug ineffective for unapproved indication
125889592 12588959 Off label use

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

no results found

Therapies reported

no results found