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
121044857 12104485 7 F 20150206 20160823 20160223 20160829 EXP JP-PFIZER INC-2016104852 PFIZER 32.00 YR F Y 44.00000 KG 20160829 MD JP JP

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
121044857 12104485 1 PS SIROLIMUS. SIROLIMUS 1 Oral 2 MG, 1X/DAY 20 MG U 21110 2 MG QD
121044857 12104485 2 SS SIROLIMUS. SIROLIMUS 1 Oral 3 MG, 1X/DAY 20 MG U 21110 3 MG QD
121044857 12104485 3 C ULTIBRO GLYCOPYRRONIUMINDACATEROL 1 Respiratory (inhalation) UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121044857 12104485 1 Lymphangioleiomyomatosis
121044857 12104485 3 Lymphangioleiomyomatosis

Outcome of event

Event ID CASEID OUTC COD
121044857 12104485 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121044857 12104485 Acne
121044857 12104485 Ascites
121044857 12104485 Condition aggravated
121044857 12104485 Constipation
121044857 12104485 Eczema
121044857 12104485 Epistaxis
121044857 12104485 Hypercholesterolaemia
121044857 12104485 Hypertriglyceridaemia
121044857 12104485 Oedema peripheral
121044857 12104485 Pleural effusion
121044857 12104485 Stomatitis
121044857 12104485 Tonsillitis
121044857 12104485 Upper respiratory tract inflammation

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
121044857 12104485 1 20150131 20150209 0
121044857 12104485 2 20150210 0