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
126097272 12609727 2 F 20160729 20160920 20160801 20160926 PER PHEH2016US019028 NOVARTIS 76.30 YR F Y 50.00000 KG 20160926 CN COUNTRY NOT SPECIFIED 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
126097272 12609727 1 PS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 25 MG, QD N 22291 25 MG TABLET QD
126097272 12609727 2 SS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 50 MG, QD N 22291 50 MG TABLET QD
126097272 12609727 3 SS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 75 MG, QD N 22291 75 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126097272 12609727 1 Immune thrombocytopenic purpura

Outcome of event

Event ID CASEID OUTC COD
126097272 12609727 HO
126097272 12609727 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126097272 12609727 Anaemia
126097272 12609727 Anxiety
126097272 12609727 Blood pressure systolic increased
126097272 12609727 Chest pain
126097272 12609727 Drug ineffective
126097272 12609727 Thrombocytopenia

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
126097272 12609727 1 20160505 20160609 0
126097272 12609727 2 20160609 20160624 0
126097272 12609727 3 20160624 20160811 0