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
126820471 12682047 1 I 20160817 20160824 20160824 EXP GB-MHRA-ROCHE-1811674 GB-FRESENIUS KABI-FK201605526 FRESENIUS KABI 0.00 F Y 0.00000 20160824 OT GB GB

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
126820471 12682047 1 PS TOPOTECAN TOPOTECANTOPOTECAN HYDROCHLORIDE 1 Unknown U UNKNOWN 91089 .75 MG/M**2 UNKNOWN
126820471 12682047 2 SS AVASTIN BEVACIZUMAB 1 Unknown 0 15 MG/M**2 UNKNOWN Q3W
126820471 12682047 3 SS TAXOL PACLITAXEL 1 Unknown 0 UNKNOWN
126820471 12682047 4 C CARBOPLATIN. CARBOPLATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126820471 12682047 1 Cervix carcinoma
126820471 12682047 2 Cervix carcinoma
126820471 12682047 3 Cervix carcinoma

Outcome of event

Event ID CASEID OUTC COD
126820471 12682047 OT
126820471 12682047 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126820471 12682047 Bone marrow failure
126820471 12682047 Death
126820471 12682047 Drug hypersensitivity
126820471 12682047 General physical health deterioration
126820471 12682047 Metastases to bone

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

no results found

Therapies reported

no results found