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
127803631 12780363 1 I 20141128 20141201 20160926 20160926 EXP PHHY2014US181362 NOVARTIS 66.81 YR F Y 0.00000 20160926 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
127803631 12780363 1 PS PROMACTA ELTROMBOPAG OLAMINE 1 Unknown UNK 5ZP8973 22291 TABLET
127803631 12780363 2 SS PROMACTA ELTROMBOPAG OLAMINE 1 22291 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127803631 12780363 1 Thrombocytopenia
127803631 12780363 2 Aplastic anaemia

Outcome of event

Event ID CASEID OUTC COD
127803631 12780363 HO
127803631 12780363 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127803631 12780363 Cough
127803631 12780363 Dyspnoea
127803631 12780363 Foot fracture
127803631 12780363 Nasopharyngitis
127803631 12780363 Oropharyngeal pain
127803631 12780363 Pulmonary arterial hypertension

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
127803631 12780363 1 20111111 0