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
124539633 12453963 3 F 20160712 20160609 20160715 EXP PHEH2016US013975 NOVARTIS 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
124539633 12453963 1 PS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 50 MG, QD 22291 50 MG TABLET QD
124539633 12453963 2 SS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 100 MG, QD (50 MG 2 TAB A DAY) 22291 100 MG TABLET QD
124539633 12453963 3 SS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 150 MG, QD 22291 150 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124539633 12453963 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124539633 12453963 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124539633 12453963 Asthenia
124539633 12453963 Back pain
124539633 12453963 Constipation
124539633 12453963 Diverticulum
124539633 12453963 Gastric disorder
124539633 12453963 Joint swelling
124539633 12453963 Malaise
124539633 12453963 Nausea
124539633 12453963 Peripheral swelling

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
124539633 12453963 1 20160510 0
124539633 12453963 2 20160511 0
124539633 12453963 3 201605 0