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
124051422 12405142 2 F 2015 20160713 20160525 20160718 PER US-CELGENEUS-USA-2015115228 CELGENE 0.00 F Y 0.00000 20160715 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
124051422 12405142 1 PS THALOMID THALIDOMIDE 1 Oral 200 MILLIGRAM U B0029AB 20785 100 MG CAPSULES BID
124051422 12405142 2 C ACTHAR CORTICOTROPIN 1 Subcutaneous 0 80 IU UNKNOWN BIW
124051422 12405142 3 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 0 200 MG UNKNOWN BID
124051422 12405142 4 C MOBIC MELOXICAM 1 Oral 0 15 MG UNKNOWN QD
124051422 12405142 5 C DECADRON DEXAMETHASONE 1 Oral 0 1 MG UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124051422 12405142 1 Subacute cutaneous lupus erythematosus
124051422 12405142 2 Systemic lupus erythematosus
124051422 12405142 3 Systemic lupus erythematosus
124051422 12405142 4 Systemic lupus erythematosus
124051422 12405142 5 Systemic lupus erythematosus

Outcome of event

Event ID CASEID OUTC COD
124051422 12405142 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124051422 12405142 Asthenia
124051422 12405142 Hypoaesthesia
124051422 12405142 Subacute cutaneous lupus erythematosus

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
124051422 12405142 1 201509 20151109 0
124051422 12405142 2 201409 201601 0
124051422 12405142 3 201308 201601 0
124051422 12405142 4 201504 201601 0
124051422 12405142 5 201404 201601 0