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
126702891 12670289 1 I 20160315 20160809 20160821 20160821 EXP AU-009507513-1608AUS006136 MERCK 4.67 YR F Y 20.00000 KG 20160821 OT AU AU

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
126702891 12670289 1 PS ELOCON MOMETASONE FUROATE 1 Topical UNK UNK, TID 19625 CREAM TID
126702891 12670289 2 SS HYDROCORTISONE. HYDROCORTISONE 1 Topical UNK 0 CREAM
126702891 12670289 3 SS ADVANTAN CORTICOSTEROID NOS 1 Topical UNK 0
126702891 12670289 4 C CLARATYNE LORATADINE 1 0
126702891 12670289 5 C DAIVOBET BETAMETHASONE DIPROPIONATECALCIPOTRIENE 1 0
126702891 12670289 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126702891 12670289 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126702891 12670289 Erythema
126702891 12670289 Insomnia
126702891 12670289 Pruritus
126702891 12670289 Wound secretion

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
126702891 12670289 1 20160307 0
126702891 12670289 2 20110315 20160307 0
126702891 12670289 3 20160307 0