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
117741618 11774161 8 F 20151007 20160909 20151124 20160919 EXP US-PFIZER INC-2015391798 PFIZER 18.00 YR M Y 109.00000 KG 20160919 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
117741618 11774161 1 PS CRIZOTINIB CRIZOTINIB 1 Oral 250 MG, CYCLIC (2X/DAY) ON DAY 1-21 (COURSE A, B) 7250 MG Y 202570 250 MG
117741618 11774161 2 SS CYTARABINE. CYTARABINE 1 Intrathecal UNK, CYCLIC (ON DAY 1, PRO-PHASE) 1400 MG 72168 SOLUTION FOR INJECTION
117741618 11774161 3 SS CYTARABINE. CYTARABINE 1 Intravenous (not otherwise specified) UNK, CYCLIC, OVER 1-30 MINUTES EVERY 12 HOURS ON DAYS 4, 5 (COURSE A) 1400 MG 72168 SOLUTION FOR INJECTION
117741618 11774161 4 SS DOXORUBICIN HCL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNK, CYCLIC, ON DAYS 4 AND 5 (COURSE B) 120 MG 50467
117741618 11774161 5 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intrathecal UNK, CYCLIC (ON DAY 1 PRO-PHASE) 7080 MG 11719
117741618 11774161 6 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Intravenous (not otherwise specified) UNK, CYCLIC, OVER 3 HOURS (COURSE A, B) 7080 MG 11719
117741618 11774161 7 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) UNK, CYCLIC, (PROPHASE, COURSE B) 2350 MG 0
117741618 11774161 8 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral UNK, CYCLIC (PROPHASE, COURSE A, B) 120 MG 0
117741618 11774161 9 SS IFOSFAMIDE. IFOSFAMIDE 1 Intravenous (not otherwise specified) UNK, CYCLIC, OVER 60 MIN ON DAY 1-5 (COURSE A) 9350 MG 0
117741618 11774161 10 C HYDROCORTISONE ACETATE. HYDROCORTISONE ACETATE 1 Intrathecal 7.5-12MG, ON DAY 1 (PROPHASE) 0
117741618 11774161 11 C VP-16 ETOPOSIDE 1 Intravenous (not otherwise specified) 100 MG/M2, CYCLIC, ON DAYS 4 AND 5 (COURSE A) 0 100 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117741618 11774161 1 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 2 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 4 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 5 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 7 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 8 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 9 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 10 Anaplastic large cell lymphoma T- and null-cell types
117741618 11774161 11 Anaplastic large cell lymphoma T- and null-cell types

Outcome of event

Event ID CASEID OUTC COD
117741618 11774161 OT
117741618 11774161 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117741618 11774161 Enterocolitis
117741618 11774161 Hypokalaemia
117741618 11774161 Lung infection
117741618 11774161 Nausea
117741618 11774161 Pleural effusion
117741618 11774161 Stomatitis
117741618 11774161 Vomiting

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
117741618 11774161 1 20150908 20151013 0
117741618 11774161 2 20150903 0
117741618 11774161 3 20150911 0
117741618 11774161 4 20151002 0
117741618 11774161 5 20150903 0
117741618 11774161 7 20150903 0
117741618 11774161 8 20150903 0
117741618 11774161 9 20150908 0
117741618 11774161 10 20150903 20150903 0
117741618 11774161 11 20150911 20150912 0