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
124517756 12451775 6 F 20160604 20160823 20160609 20160824 PER GB-EISAI MEDICAL RESEARCH-EC-2016-017525 EISAI 69.22 YR M Y 85.00000 KG 20160824 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
124517756 12451775 1 PS LENVATINIB LENVATINIB 1 Oral Y N 206947 12 MG CAPSULE QD
124517756 12451775 2 SS LENVATINIB LENVATINIB 1 Oral Y N 206947 12 MG CAPSULE QD
124517756 12451775 3 SS PERINDOPRIL PERINDOPRIL 1 Oral 0 4 MG TABLET QD
124517756 12451775 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
124517756 12451775 5 C THYROXINE LEVOTHYROXINE 1 0
124517756 12451775 6 C ATORVASTATIN ATORVASTATIN 1 0
124517756 12451775 7 C IBUPROFEN. IBUPROFEN 1 0
124517756 12451775 8 C ZOPLICONE ZOPICLONE 1 0
124517756 12451775 9 C QUININE SULPHATE QUININE SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124517756 12451775 1 Hepatocellular carcinoma
124517756 12451775 3 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
124517756 12451775 LT
124517756 12451775 OT
124517756 12451775 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124517756 12451775 Haematuria
124517756 12451775 Hyperkalaemia
124517756 12451775 Hypocalcaemia
124517756 12451775 Hypomagnesaemia

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
124517756 12451775 1 20150707 20160606 0
124517756 12451775 2 20160711 0
124517756 12451775 3 20160705 0