The Safety Rates Drug Report

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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
125275121 12527512 1 I 20160526 20160705 20160705 EXP NZ-ACTAVIS-2016-14655 ACTAVIS TAGHAVI K, SYKES P, INNES C, GIBBS D, HUNTER L, MCBURNIE W ET AL. WRONG PLACE AT THE WRONG TIME: A CASE OF CERVICAL EMBRYONAL RHABDOMYOSARCOMA IN PREGNANCY. GYNECOL ONCOL REP. 2015;12:77-9. 36.00 YR F Y 0.00000 20160705 MD NZ NZ

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
125275121 12527512 1 PS Doxorubicin (Unknown) DOXORUBICIN 1 Unknown ADMINISTERED WITHIN 2 DAYS AND 21 DAYS BETWEEN EACH ROUND OFF 6 ROUNDS U UNCONFIRMED 203622 .75 MG/M**2 UNK
125275121 12527512 2 SS Vincristine (Unknown) VINCRISTINE 1 Unknown ADMINISTERED WITHIN 2 DAYS AND 21 DAYS BETWEEN EACH ROUND OFF 6 ROUNDS U UNCONFIRMED 0 1.4 MG/M**2 UNK
125275121 12527512 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown ADMINISTERED WITHIN 2 DAYS AND 21 DAYS BETWEEN EACH ROUND OFF 6 ROUNDS U 0 1500 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125275121 12527512 1 Embryonal rhabdomyosarcoma
125275121 12527512 2 Embryonal rhabdomyosarcoma
125275121 12527512 3 Embryonal rhabdomyosarcoma

Outcome of event

Event ID CASEID OUTC COD
125275121 12527512 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125275121 12527512 Exposure during pregnancy
125275121 12527512 Memory impairment
125275121 12527512 Neutropenia

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

no results found

Therapies reported

no results found