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
126797052 12679705 2 F 20160802 20160830 20160824 20160907 EXP CA-ROCHE-1818957 ROCHE 66.04 YR M Y 0.00000 20160907 MD CA 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
126797052 12679705 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous 150 MG, EVERY 4 WEEKS U 103976 150 MG SOLUTION FOR INJECTION
126797052 12679705 2 SS METOPROLOL. METOPROLOL 1 Unknown 50 MG, BID 0 50 MG BID
126797052 12679705 3 SS METOPROLOL. METOPROLOL 1 Subcutaneous 37 MG, BID (DOSE DECREASE FROM 100 MG TO 75 MG) 0 37 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126797052 12679705 1 Asthma
126797052 12679705 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126797052 12679705 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126797052 12679705 Atrial fibrillation
126797052 12679705 Dyspnoea
126797052 12679705 Forced expiratory volume decreased
126797052 12679705 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
126797052 12679705 1 20140319 0
126797052 12679705 2 2016 0