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
122699062 12269906 2 F 201402 20160803 20160415 20160804 EXP DE-ROCHE-1672432 ROCHE 47.00 YR F Y 0.00000 20160804 MD DE DE

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
122699062 12269906 1 PS Tocilizumab TOCILIZUMAB 1 Subcutaneous N 125472 480 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
122699062 12269906 2 SS Tocilizumab TOCILIZUMAB 1 Subcutaneous N 125472 162 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
122699062 12269906 3 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 0
122699062 12269906 4 C TOPIRAMAT TOPIRAMATE 1 0
122699062 12269906 5 C PREDNISOLONE. PREDNISOLONE 1 0
122699062 12269906 6 C ALENDRONIC ACID ALENDRONIC ACID 1 0
122699062 12269906 7 C ZOLMITRIPTAN. ZOLMITRIPTAN 1 0
122699062 12269906 8 C TILIDIN COMP NALOXONE HYDROCHLORIDETILIDINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122699062 12269906 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122699062 12269906 HO
122699062 12269906 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122699062 12269906 Depression
122699062 12269906 Headache
122699062 12269906 Oral mucosal blistering
122699062 12269906 Pollakiuria

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
122699062 12269906 1 201211 0