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
127112491 12711249 1 I 20160819 20160902 20160902 EXP GB-MHRA-ADR 23603398 GB-ACCORD-043531 ACCORD 53.00 YR M Y 95.00000 KG 20160902 CN 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
127112491 12711249 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Oral ALSO RECEIVED 5 MG N 202553 10 MG
127112491 12711249 2 C ATORVASTATIN ATORVASTATIN 1 0
127112491 12711249 3 C ACETYLSALICYLIC ACID ASPIRIN 1 0
127112491 12711249 4 C CARVEDILOL/CARVEDILOL HYDROCHLODRIDE 2 0
127112491 12711249 5 C LOSARTAN. LOSARTAN 1 0
127112491 12711249 6 C OMEPRAZOLE. OMEPRAZOLE 1 0
127112491 12711249 7 C DEXCEL-PHARMA ISOSORBIDE MONONITRATE 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127112491 12711249 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127112491 12711249 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127112491 12711249 Joint swelling
127112491 12711249 Muscle spasms
127112491 12711249 Pain in extremity
127112491 12711249 Peripheral swelling

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
127112491 12711249 1 20160715 0