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
114972363 11497236 3 F 20150211 20160805 20150911 20160812 EXP US-PFIZER INC-2015297013 PFIZER 14.00 YR F Y 53.00000 KG 20160812 OT 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
114972363 11497236 1 PS CRIZOTINIB CRIZOTINIB 1 Oral COURSE A, B: 165MG/M2, BID ON DAYS 1-21 U 202570 165 MG/M**2 BID
114972363 11497236 2 SS DOXORUBICIN HCL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) COURSE B: 25 MG/M2, OVER 1-15 MIN ON DAYS 4 AND 5 U 50467 25 MG/M**2
114972363 11497236 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intrathecal PROPHASE: 7.5-12MG IT ON DAY 1 U 11719
114972363 11497236 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intravenous (not otherwise specified) COURSE A: 3000 MG/M2, OVER 3 HOURS ON DAY 1 U 11719 3000 MG/M**2
114972363 11497236 5 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intravenous (not otherwise specified) COURSE B: 3000 MG/M2, OVER 3 HOURS ON DAY 1 U 11719 3000 MG/M**2
114972363 11497236 6 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) PROPHASE: 200 MG/M2, IV OVER 15-30 MINUTES ON DAYS 1 AND 2 U 0 200 MG/M**2
114972363 11497236 7 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) COURSE B: 200MG/M2, IV OVER 15-30 MINUTES ON DAYS 1-5 U 0 200 MG/M**2
114972363 11497236 8 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral PROPHASE: 5 MG/M2, QD ON DAYS 1-2 AND BID ON DAYS 3-5 U 0 5 MG/M**2
114972363 11497236 9 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral COURSE A: 5 MG/M2, BID ON DAYS 1-5 U 0 5 MG/M**2
114972363 11497236 10 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral COURSE B: 5MG/M2 PO BID ON DAYS 1-5 U 0 5 MG/M**2
114972363 11497236 11 SS VP-16 ETOPOSIDE 1 Intravenous (not otherwise specified) COURSE A: 100 MG/M2, OVER 2 HOURS ON DAYS 4 AND 5 U 0 100 MG/M**2
114972363 11497236 12 C CYTARABINE. CYTARABINE 1 Intrathecal PROPHASE: 15-24MG ON DAY 1 0
114972363 11497236 13 C CYTARABINE. CYTARABINE 1 Intravenous (not otherwise specified) COURSE A: 150 MG/M2, OVER 1-30 MINUTES Q12 HOURS ON DAYS 4 AND 5 0 150 MG/M**2
114972363 11497236 14 C HYDROCORTISONE. HYDROCORTISONE 1 Intrathecal PROPHASE: 7.5-12 MG ON DAY 1 0
114972363 11497236 15 C IFOSFAMIDE. IFOSFAMIDE 1 Intravenous (not otherwise specified) COURSE A: 800 MG/M2, OVER 60 MINUTES ON DAYS 1-5 0 800 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114972363 11497236 1 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 2 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 3 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 6 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 8 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 11 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 12 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 14 Anaplastic large cell lymphoma T- and null-cell types
114972363 11497236 15 Anaplastic large cell lymphoma T- and null-cell types

Outcome of event

Event ID CASEID OUTC COD
114972363 11497236 OT
114972363 11497236 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114972363 11497236 Anaemia
114972363 11497236 Hypokalaemia
114972363 11497236 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found