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
127184842 12718484 2 F 20160529 20160901 20160906 20160908 EXP IT-ALLERGAN-1667740US ALLERGAN 51.00 YR M Y 0.00000 20160908 MD IT IT

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
127184842 12718484 1 PS SUCRALFATE Unk SUCRALFATE 1 Oral UNK Y 19183
127184842 12718484 2 C MICARDIS TELMISARTAN 1 U 0
127184842 12718484 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 U 0
127184842 12718484 4 C GLICLAZIDE GLICLAZIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127184842 12718484 1 Product used for unknown indication
127184842 12718484 2 Product used for unknown indication
127184842 12718484 3 Diabetes mellitus
127184842 12718484 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127184842 12718484 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127184842 12718484 Erythema
127184842 12718484 Face oedema
127184842 12718484 Pruritus

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
127184842 12718484 1 20160527 20160529 0