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
127912721 12791272 1 I 201309 20160921 20160929 20160929 EXP PHHY2016GB130580 SANDOZ 49.00 YR M Y 0.00000 20160929 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
127912721 12791272 1 PS SALBUTAMOL ALBUTEROL 1 Unknown U U 72151
127912721 12791272 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 2 DF, BID,2 PUFF(S), BID U U 0 2 DF BID
127912721 12791272 3 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 DF, BID,1 PUFF(S), BID U U 0 1 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127912721 12791272 1 Asthma
127912721 12791272 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
127912721 12791272 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127912721 12791272 Asthma
127912721 12791272 Circulatory collapse
127912721 12791272 Concussion
127912721 12791272 Dizziness
127912721 12791272 Fall
127912721 12791272 Hyperinsulinaemia
127912721 12791272 Hypokalaemic syndrome
127912721 12791272 Intentional product misuse
127912721 12791272 Joint lock
127912721 12791272 Orthostatic hypertension
127912721 12791272 Paralysis
127912721 12791272 Stress

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
127912721 12791272 3 2001 0