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
127200511 12720051 1 I 20160818 20160826 20160907 20160907 EXP GB-MHRA-ADR 23614171 GB-ACCORD-043708 ACCORD 68.00 YR F Y 82.00000 KG 20160907 MD 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
127200511 12720051 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 78155 40 MG
127200511 12720051 2 C BETAHISTINE BETAHISTINE 1 719.88 DF 0 1 DF TID
127200511 12720051 3 C BUDESONIDE. BUDESONIDE 1 USE AS DIRECTED 0
127200511 12720051 4 C SALBUTAMOL ALBUTEROL 1 Respiratory (inhalation) 0 2 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127200511 12720051 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127200511 12720051 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127200511 12720051 Pain

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
127200511 12720051 1 20160818 0
127200511 12720051 2 20151222 0
127200511 12720051 3 20150715 0
127200511 12720051 4 20150715 0