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
126273811 12627381 1 I 201606 20160720 20160805 20160805 PER US-AMGEN-USASL2016094676 AMGEN 49.00 YR A M Y 0.00000 20160805 OT 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
126273811 12627381 1 PS NPLATE ROMIPLOSTIM 1 Unknown UNK UNK, QWK 125268 POWDER FOR INJECTION /wk
126273811 12627381 2 SS NPLATE ROMIPLOSTIM 1 Unknown 800 MUG, UNK 125268 800 UG POWDER FOR INJECTION
126273811 12627381 3 SS VINCRISTINE VINCRISTINE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126273811 12627381 1 Immune thrombocytopenic purpura
126273811 12627381 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126273811 12627381 Contusion
126273811 12627381 Epistaxis
126273811 12627381 Fatigue
126273811 12627381 Headache
126273811 12627381 Hypotension
126273811 12627381 Insomnia
126273811 12627381 Pain in extremity
126273811 12627381 Petechiae
126273811 12627381 Purpura
126273811 12627381 Stomatitis
126273811 12627381 Therapeutic response unexpected
126273811 12627381 Urticaria

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
126273811 12627381 1 201512 0
126273811 12627381 2 201607 0