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
93834074 9383407 4 F 20130627 20160920 20130704 20160922 EXP CA-ROCHE-1244254 ROCHE 13.07 YR M Y 0.00000 20160922 OT 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
93834074 9383407 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0003C 103976 225 MG SOLUTION FOR INJECTION BIW
93834074 9383407 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0003C 103976 225 MG SOLUTION FOR INJECTION BIW
93834074 9383407 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0003C 103976 SOLUTION FOR INJECTION
93834074 9383407 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0003C 103976 SOLUTION FOR INJECTION
93834074 9383407 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0003C 103976 SOLUTION FOR INJECTION
93834074 9383407 6 C ZENHALE FORMOTEROL FUMARATEMOMETASONE FUROATE 1 0
93834074 9383407 7 C VENTOLIN ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93834074 9383407 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
93834074 9383407 HO
93834074 9383407 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93834074 9383407 Blood pressure decreased
93834074 9383407 Epilepsy
93834074 9383407 Weight increased

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
93834074 9383407 1 20130530 0
93834074 9383407 2 20130627 0
93834074 9383407 3 20140403 0
93834074 9383407 4 201606 0
93834074 9383407 5 20160901 0