The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5117580 6139098 I 5117580-3 20060919 20060929 EXP FR-ROCHE-463820 ROCHE 53 YR F Y 20060929 MD FRANCE

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5117580 1007716921 PS GANCICLOVIR 1 UNKNOWN SECOND THERAPY. STARTED FIVE DAYS AFTER FIRST THERAPY WAS STOPPED. 20460
5117580 1007716922 SS GANCICLOVIR 1 UNKNOWN 020460
5117580 1007716923 SS ARGININE BUTYRATE 2 UNKNOWN DRUG NAME: ARGININE BUTYRATE. ESCALATING DOSE OF LESS THAN OR EQUAL TO 1500 MG/KG. SECOND THERAPY S+
5117580 1007716924 SS ARGININE BUTYRATE 2 UNKNOWN DRUG NAME: ARGININE BUTYRATE. ESCALATING DOSE OF LESS THAN OR EQUAL TO 1500 MG/KG.
5117580 1007716925 C ADRIAMYCIN PFS 1 THE PATIENT RECEIVED FOUR CYCLES OF TREATMENT IN COMBINATION WITH CYCLOPHOSPHAMIDE/BLEOMYCIN AND PR+
5117580 1007716926 C CYCLOPHOSPHAMIDE 1 THE PATIENT RECEIVED FOUR CYCLES OF TREATMENT IN COMBINATION WITH ADRIAMYCIN, BLEOMYCIN AND PREDNIS+
5117580 1007716927 C BLEOMYCIN 1 THE PATIENT RECEIVED FOUR CYCLES OF TREATMENT IN COMBINATION WITH ADRIAMYCIN, CYCLOPHOSPHAMIDE AND +
5117580 1007716928 C PREDNISONE TAB 1 THE PATIENT RECEIVED FOUR CYCLES OF TREATMENT IN COMBINATION WITH ADRIAMYCIN, CYCLOPHOSPHAMIDE AND +
5117580 1007716929 C CISPLATIN 1 SECOND LINE CHEMOTHERAPY IN COMBINATION WITH CYTOSINE ARABINOSIDE AND PREDNISOLONE.
5117580 1007716930 C CYTOSINE ARABINOSIDE 2 SECOND LINE CHEMOTHERAPY IN COMBINATION WITH CYTOSINE ARABINOSIDE AND PREDNISOLONE.
5117580 1007716931 C PREDNISOLONE 1 SECOND LINE CHEMOTHERAPY IN COMBINATION WITH CYTOSINE ARABINOSIDE AND PREDNISOLONE.

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5117580 DE

Reactions reported

Event ID PT
5117580 HEPATITIS

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5117580 1007716922 12 DAY
5117580 1007716924 12 DAY