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
107927162 10792716 2 F 20150115 20160712 20150213 20160718 EXP PHHO2015FR001226 NOVARTIS 61.00 YR F Y 0.00000 20160718 MD FR FR

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
107927162 10792716 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 22334 10 MG TABLET QD
107927162 10792716 2 C DIFFU-K POTASSIUM CHLORIDE 1 Oral 8 DF, QD 0 8 DF CAPSULE QD
107927162 10792716 3 C LODOZ BISOPROLOL FUMARATEHYDROCHLOROTHIAZIDE 1 Oral 1 DF, QD (5MG/6.25MG) 0 1 DF FILM-COATED TABLET QD
107927162 10792716 4 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 Oral 1 DF, QD (60 MG, 1 DF DAILY) U 0 1 DF FILM-COATED TABLET QD
107927162 10792716 5 C CALCIDOSE VITAMINE D CALCIUMCHOLECALCIFEROL 1 Oral 2 DF, QD (500MG/400 IU) 0 2 DF SACHET BID
107927162 10792716 6 C DIAMICRON GLICLAZIDE 1 Oral 60 MG U 0 60 MG TABLET
107927162 10792716 7 C LEVOTHYROX LEVOTHYROXINE 1 Unknown 87.5 UG, QD 0 87.5 UG QD
107927162 10792716 8 C SANDOSTATIN OCTREOTIDE ACETATE 1 Unknown 120 MG, QMO U 0 120 MG POWDER FOR SOL FOR INJ /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107927162 10792716 1 Metastases to liver
107927162 10792716 2 Product used for unknown indication
107927162 10792716 3 Product used for unknown indication
107927162 10792716 4 Product used for unknown indication
107927162 10792716 5 Product used for unknown indication
107927162 10792716 6 Product used for unknown indication
107927162 10792716 7 Product used for unknown indication
107927162 10792716 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
107927162 10792716 DS
107927162 10792716 DE
107927162 10792716 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
107927162 10792716 Anaemia
107927162 10792716 Death
107927162 10792716 Hepatic cirrhosis

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
107927162 10792716 1 20140206 20150116 0
107927162 10792716 4 201411 0
107927162 10792716 6 20150116 0