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
116895283 11689528 3 F 20151022 20151216 20151102 20160928 PER PHEH2015US021824 NOVARTIS 16.22 YR F Y 0.00000 20160928 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
116895283 11689528 1 PS PROMACTA ELTROMBOPAG OLAMINE 1 Oral 150 MG, UNK Y 22291 150 MG
116895283 11689528 2 SS CICLOSPORIN A CYCLOSPORINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116895283 11689528 1 Aplastic anaemia
116895283 11689528 2 Aplastic anaemia

Outcome of event

Event ID CASEID OUTC COD
116895283 11689528 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116895283 11689528 Acanthosis
116895283 11689528 Drug administered to patient of inappropriate age
116895283 11689528 Eczema
116895283 11689528 Glossodynia
116895283 11689528 Lymphocytic infiltration
116895283 11689528 Malaise
116895283 11689528 Oral pain
116895283 11689528 Oropharyngeal pain
116895283 11689528 Pruritus
116895283 11689528 Pyrexia
116895283 11689528 Rash maculo-papular
116895283 11689528 Swelling face

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
116895283 11689528 1 20150925 20151022 0