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
124913933 12491393 3 F 2016 20160804 20160623 20160809 EXP US-009507513-1606USA009517 MERCK 91.64 YR M Y 0.00000 20160809 CN 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
124913933 12491393 1 PS DEXAMETHASONE. DEXAMETHASONE 1 EVERY WEEK U 12675 TABLET /wk
124913933 12491393 2 SS DEXAMETHASONE. DEXAMETHASONE 1 16 MG, QW U 12675 16 MG TABLET /wk
124913933 12491393 3 SS REVLIMID LENALIDOMIDE 1 Oral 25 MG, QD 330 MG U 0 25 MG CAPSULE QD
124913933 12491393 4 SS REVLIMID LENALIDOMIDE 1 Oral 15 MG, QD 330 MG U 0 15 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124913933 12491393 1 Product used for unknown indication
124913933 12491393 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
124913933 12491393 DE
124913933 12491393 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124913933 12491393 Decreased appetite
124913933 12491393 Fatigue
124913933 12491393 Haematocrit decreased
124913933 12491393 Haemoglobin decreased
124913933 12491393 Muscular weakness
124913933 12491393 Peripheral swelling
124913933 12491393 Plasma cell myeloma
124913933 12491393 White blood cell count 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
124913933 12491393 1 2016 0
124913933 12491393 2 2016 0
124913933 12491393 3 201601 0
124913933 12491393 4 20160204 20160225 0