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
127781651 12778165 1 I 20160915 20160925 20160925 EXP PHHY2016GB127855 SANDOZ 0.00 F Y 0.00000 20160926 OT 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
127781651 12778165 1 PS SALBUTAMOL ALBUTEROL 1 Unknown U U 72151
127781651 12778165 2 SS DUORESP SPIROMAX BUDESONIDEFORMOTEROL 1 Unknown 320 UG U U AEW54A 0 320 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127781651 12778165 1 Product used for unknown indication
127781651 12778165 2 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
127781651 12778165 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127781651 12778165 Drug ineffective
127781651 12778165 Dyspnoea
127781651 12778165 Headache
127781651 12778165 Malaise
127781651 12778165 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found