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
125864191 12586419 1 I 20160618 0 20160722 20160722 DIR 68.63 YR F N 52.30000 KG 20160718 N MD 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
125864191 12586419 1 PS METHOTREXATE. METHOTREXATE 1 0 7770 MG
125864191 12586419 3 C RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMERIC) RITUXIMAB 1 0 1530 MG
125864191 12586419 5 C PROCARBAZINE PROCARBAZINE 1 0 550 MG
125864191 12586419 6 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125864191 12586419 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125864191 12586419 Disease progression
125864191 12586419 Dizziness
125864191 12586419 Gait disturbance
125864191 12586419 Headache
125864191 12586419 Hyponatraemia
125864191 12586419 Pneumonia
125864191 12586419 Urinary retention
125864191 12586419 Vertigo
125864191 12586419 Visual impairment

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
125864191 12586419 1 20160517 0
125864191 12586419 3 20160516 0
125864191 12586419 5 20160509 0
125864191 12586419 6 20160114 0