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
125988121 12598812 1 I 2010 20151102 20160727 20160727 EXP US-GLAXOSMITHKLINE-CHPA2015US013047 GLAXOSMITHKLINE 0.00 Y 0.00000 20160727 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
125988121 12598812 1 PS VOLTAREN DICLOFENAC SODIUM 1 Topical 10 G, QD UNK 22122 10 G GEL QD
125988121 12598812 2 C DOXIL DOXORUBICIN HYDROCHLORIDE 1 UNK, 1-2 WEEKLY Y 0
125988121 12598812 3 C VINCRISTINE VINCRISTINE 1 UNK, 1-2 WEKLY Y UNK 0
125988121 12598812 4 C DEXAMETHASONE. DEXAMETHASONE 1 UNK, 1-2 WEEKLY Y UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125988121 12598812 1 Osteoarthritis
125988121 12598812 2 Plasma cell myeloma
125988121 12598812 3 Plasma cell myeloma
125988121 12598812 4 Plasma cell myeloma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125988121 12598812 Drug administered at inappropriate site
125988121 12598812 Inappropriate schedule of drug administration
125988121 12598812 Middle insomnia
125988121 12598812 Underdose

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
125988121 12598812 1 201001 0
125988121 12598812 2 201506 201510 0
125988121 12598812 3 201506 201510 0
125988121 12598812 4 201506 201510 0