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
127249541 12724954 1 I 20160101 20160831 20160908 20160908 EXP NL-LRB-224444 PHHY2016NL119897 SANDOZ 19.00 YR F Y 65.00000 KG 20160908 OT NL NL

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
127249541 12724954 1 PS SALBUTAMOL SANDOZ ALBUTEROL 1 Respiratory (inhalation) 400 UG N 72151 400 UG AEROSOL
127249541 12724954 2 C FOSTER BECLOMETHASONEFORMOTEROL 1 Respiratory (inhalation) 2 DF, TID N 0 2 DF AEROSOL TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127249541 12724954 1 Asthma
127249541 12724954 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127249541 12724954 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127249541 12724954 Asthma
127249541 12724954 General physical health deterioration
127249541 12724954 Palpitations
127249541 12724954 Product quality issue
127249541 12724954 Therapeutic response decreased
127249541 12724954 Therapeutic response unexpected

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
127249541 12724954 1 20160101 0
127249541 12724954 2 2016 20160822 0