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
127083111 12708311 1 I 20160818 20160826 20160901 20160901 EXP GB-MHRA-TPP10419171C2710752YC1471514489913 GB-MYLANLABS-2016M1036854 MYLAN 0.00 Y 0.00000 20160901 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
127083111 12708311 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG, UNK U 90868 40 MG
127083111 12708311 2 C BETAHISTINE BETAHISTINE 1 1 DF, TID 719.875 DF U 0 1 DF TID
127083111 12708311 3 C BUDESONIDE. BUDESONIDE 1 UNK (USE AS DIRECTED) U 0
127083111 12708311 4 C SALBUTAMOL ALBUTEROL 1 Respiratory (inhalation) 2 DF, UNK U 0 2 DF

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127083111 12708311 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127083111 12708311 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
127083111 12708311 1 20160818 0
127083111 12708311 2 20151222 0
127083111 12708311 3 20150715 0
127083111 12708311 4 20150715 0