The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
5117318 6138945 F 5117318-X 20060404 20060404 20060929 EXP GB-BAYER-200610414BNE BAYER PHARMACEUTICALS CORPORATION 31 YR M Y 75 KG 20060929 UNITED KINGDOM

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
5117318 1007715819 PS SORAFENIB 2 ORAL 21923
5117318 1007715820 SS DACARBAZINE 1 INTRAVENOUS 017575
5117318 1007715821 C FERROUS SULFATE TAB 1 ORAL
5117318 1007715822 C OMEPRAZOLE 1 ORAL
5117318 1007715823 C TRANEXAMIC ACID 2 ORAL
5117318 1007715824 C CEPHALEXIN 1 ORAL
5117318 1007715825 C MILPAR 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5117318 1007715819 METASTATIC MALIGNANT MELANOMA
5117318 1007715820 METASTATIC MALIGNANT MELANOMA
5117318 1007715821 ANAEMIA
5117318 1007715822 DYSPEPSIA
5117318 1007715823 HAEMORRHAGE
5117318 1007715824 URINARY TRACT INFECTION
5117318 1007715825 CONSTIPATION

Outcome of event

Event ID OUTC COD
5117318 HO
5117318 LT
5117318 OT

Reactions reported

Event ID PT
5117318 ANAEMIA
5117318 SMALL INTESTINAL HAEMORRHAGE

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
5117318 1007715819 20050907 20060405 211 DAY
5117318 1007715820 20060315 20060315 1 DAY
5117318 1007715821 20050824
5117318 1007715822 20050824
5117318 1007715823 20050824
5117318 1007715824 20050901
5117318 1007715825 20050824