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
125820631 12582063 1 I 20160219 20160722 20160722 PER US-STRIDES ARCOLAB LIMITED-2016SP001201 STRIDES 0.00 Y 0.00000 20160722 MD US US

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
125820631 12582063 1 PS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 500 MG, BID 90055 500 MG
125820631 12582063 2 SS PREDNISOLONE. PREDNISOLONE 1 15 MG, QD 0 15 MG
125820631 12582063 3 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 400 MG, QD 0 400 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125820631 12582063 1 Systemic lupus erythematosus
125820631 12582063 2 Systemic lupus erythematosus
125820631 12582063 3 Systemic lupus erythematosus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125820631 12582063 Exposure during pregnancy
125820631 12582063 Off label use

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
125820631 12582063 1 2014 0
125820631 12582063 3 2014 0