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
97847212 9784721 2 F 20081125 20151204 20131227 20160830 EXP GB-ROCHE-1326026 ROCHE 63.00 YR M Y 0.00000 20160830 MD 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
97847212 9784721 1 PS CAPECITABINE. CAPECITABINE 1 Oral ON DAY 1-21 U 20896 BID
97847212 9784721 2 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 30 MIN ON DAY 1, 8 AND 15 U 0
97847212 9784721 3 C URSODEOXYCHOLIC ACID URSODIOL 1 0
97847212 9784721 4 C FENTANYL. FENTANYL 1 Unknown 0
97847212 9784721 5 C HIBISCRUB CHLORHEXIDINE GLUCONATE 1 0
97847212 9784721 6 C MEGACE MEGESTROL ACETATE 1 0
97847212 9784721 7 C AMLODIPINE AMLODIPINE BESYLATE 1 0
97847212 9784721 8 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97847212 9784721 1 Pancreatic carcinoma
97847212 9784721 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97847212 9784721 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97847212 9784721 Anaemia
97847212 9784721 Chills
97847212 9784721 Clostridium difficile infection
97847212 9784721 Diarrhoea
97847212 9784721 Neutropenic sepsis
97847212 9784721 Pyrexia
97847212 9784721 Thrombocytopenia
97847212 9784721 Vomiting

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

no results found

Therapies reported

no results found