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
126078792 12607879 2 F 20160728 20160729 20160805 EXP IT-FRESENIUS KABI-FK201604861 FRESENIUS KABI 0.00 F Y 70.00000 KG 20160805 OT IT IT

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
126078792 12607879 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Unknown Y U UNKNOWN 90242 UNKNOWN
126078792 12607879 2 SS HERCEPTIN TRASTUZUMAB 1 0 CONCENTRATE FOR SOLUTION FOR INFUSION
126078792 12607879 3 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 0
126078792 12607879 4 C CONTRAMAL TRAMADOL HYDROCHLORIDE 1 0
126078792 12607879 5 C ACETAMINOPHEN AND CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126078792 12607879 1 Breast cancer stage IV
126078792 12607879 2 Breast cancer stage IV
126078792 12607879 3 Diabetes mellitus
126078792 12607879 4 Pain
126078792 12607879 5 Pain

Outcome of event

Event ID CASEID OUTC COD
126078792 12607879 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126078792 12607879 Aphonia
126078792 12607879 Arthralgia
126078792 12607879 Cholangiectasis acquired
126078792 12607879 Dizziness
126078792 12607879 Dyspnoea exertional
126078792 12607879 Pleural effusion

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

no results found

Therapies reported

no results found