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
126785292 12678529 2 F 20160802 20160830 20160823 20160907 EXP PHHY2016CA115075 SANDOZ 66.04 YR M Y 0.00000 20160907 CN COUNTRY NOT SPECIFIED CA

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
126785292 12678529 1 SS XOLAIR OMALIZUMAB 1 Subcutaneous 150 MG, EVERY 4 WEEKS U 0 150 MG
126785292 12678529 2 PS METOPROLOL. METOPROLOL 1 Unknown 50 MG, BID Y 73288 50 MG BID
126785292 12678529 3 SS METOPROLOL. METOPROLOL 1 Subcutaneous 37 MG, BID (DOSE DECREASE FROM 100 MG TO 75 MG) Y 73288 37 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126785292 12678529 1 Asthma
126785292 12678529 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126785292 12678529 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126785292 12678529 Atrial fibrillation
126785292 12678529 Dyspnoea
126785292 12678529 Forced expiratory volume decreased
126785292 12678529 Hypopnoea

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
126785292 12678529 1 20140319 0
126785292 12678529 2 2016 0