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
1187147610 11871476 10 F 20150305 20160811 20151228 20160823 EXP JP-PFIZER INC-2015471463 PFIZER 65.00 YR F Y 61.00000 KG 20160823 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
1187147610 11871476 1 PS SIROLIMUS. SIROLIMUS 1 Oral 1 MG, 1X/DAY (1 D) 216 MG Y 21110 1 MG QD
1187147610 11871476 2 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 5 UG, 1X/DAY (1 D) 0 5 UG QD
1187147610 11871476 3 C ONBREZ INDACATEROL 1 Unknown 150 UG, 1X/DAY (1 D) 0 150 UG QD
1187147610 11871476 4 C UNIPHYLLA THEOPHYLLINE ANHYDROUS 1 Oral 200 MG, 1X/DAY (1 D) 0 200 MG QD
1187147610 11871476 5 C VITANEURIN /02072701/ 2 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1187147610 11871476 1 Lymphangioma
1187147610 11871476 2 Lymphangioleiomyomatosis
1187147610 11871476 5 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
1187147610 11871476 HO
1187147610 11871476 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1187147610 11871476 Anti-neutrophil cytoplasmic antibody positive vasculitis
1187147610 11871476 Pleural effusion
1187147610 11871476 Pneumonia
1187147610 11871476 Stomatitis

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
1187147610 11871476 1 20150305 20151006 0
1187147610 11871476 2 20150622 0
1187147610 11871476 4 20151207 0
1187147610 11871476 5 20150205 20150810 0