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
127214271 12721427 1 I 20160318 20160831 20160907 20160907 EXP NL-LRB-224792 PHHY2016NL119964 SANDOZ 9.35 YR F Y 23.00000 KG 20160907 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
127214271 12721427 1 PS SALBUTAMOL SANDOZ ALBUTEROL 1 Respiratory (inhalation) WANNEER NODIG, MAX 8 X PER DAG N 72151 1 DF AEROSOL
127214271 12721427 2 C FLIXOTIDE FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 2 KEER PER DAG 2 STUK(S) U 0 2 DF AEROSOL BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127214271 12721427 1 Asthma
127214271 12721427 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127214271 12721427 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127214271 12721427 Therapeutic response decreased
127214271 12721427 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
127214271 12721427 1 2015 20160326 0
127214271 12721427 2 20080101 0