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
126287551 12628755 1 I 20160726 20160808 20160808 EXP GB-MHRA-ADR 23571198 GB-ACCORD-042823 ACCORD 80.00 YR F Y 0.00000 20160808 PH 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
126287551 12628755 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Y 202553
126287551 12628755 2 SS PREDNISOLONE. PREDNISOLONE 1 Oral EVERY MORNING OM Y 0 10 MG QD
126287551 12628755 3 C DIHYDROCODEINE DIHYDROCODEINE 1 Oral 30MG - 60MG THREE TIMES A DAY 0
126287551 12628755 4 C ENOXAPARIN ENOXAPARIN 1 Subcutaneous 60MG/0.6ML UNTIL INRWITHIN RANGE 0
126287551 12628755 5 C FENBID IBUPROFEN 1 Topical 0
126287551 12628755 6 C LANSOPRAZOLE. LANSOPRAZOLE 1 Oral 0 30 MG QD
126287551 12628755 7 C PARACETAMOL ACETAMINOPHEN 1 Oral 0 1 G QID
126287551 12628755 8 C WARFARIN WARFARIN 1 Oral AS PER INR BOOKLET 0 1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126287551 12628755 1 Product used for unknown indication
126287551 12628755 2 Rheumatoid arthritis
126287551 12628755 8 Deep vein thrombosis

Outcome of event

Event ID CASEID OUTC COD
126287551 12628755 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126287551 12628755 Acute kidney injury
126287551 12628755 International normalised ratio increased
126287551 12628755 Joint swelling
126287551 12628755 Peripheral swelling
126287551 12628755 Polyarthritis

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
126287551 12628755 2 20160520 0