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
76760055 7676005 5 F 201010 20130925 20101119 20130930 EXP GB-JNJFOC-20101104173 JANSSEN 23.16 YR F Y 80.30000 KG 20130930 OT GB GB

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
76760055 7676005 1 PS STELARA 1 SUBCUTANEOUS U 0 45 MG LIQUID
76760055 7676005 2 SS STELARA 1 SUBCUTANEOUS U 0 45 MG LIQUID
76760055 7676005 3 SS STELARA 1 SUBCUTANEOUS U 125261 45 MG LIQUID
76760055 7676005 4 SS ERYTHROMYCIN 1 UNKNOWN D 0 UNSPECIFIED
76760055 7676005 5 C YASMIN 1 ORAL D 0 TABLETS
76760055 7676005 6 C XENICAL 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
76760055 7676005 1 Psoriasis
76760055 7676005 2 Psoriasis
76760055 7676005 3 Psoriasis
76760055 7676005 4 Product used for unknown indication
76760055 7676005 5 Contraception
76760055 7676005 6 Overweight

Outcome of event

Event ID CASEID OUTC COD
76760055 7676005 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
76760055 7676005 Alanine aminotransferase increased

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
76760055 7676005 1 20100909 0
76760055 7676005 2 20101230 0
76760055 7676005 3 20101007 0
76760055 7676005 5 20101120 0