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
126526431 12652643 1 I 20160707 20160808 20160815 20160815 EXP GB-MHRA-MIDB-4630A4D7-DEB2-4244-9E5B-9DC18BE647B2 GB-SA-2016SA145954 AVENTIS 73.00 YR E M Y 0.00000 20160815 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
126526431 12652643 1 PS INDAPAMIDE. INDAPAMIDE 1 Unknown Y UNK 18538 2.5 MG QD
126526431 12652643 2 C IRBESARTAN. IRBESARTAN 1 0 150 MG QD
126526431 12652643 3 C LEVOTHYROXINE. LEVOTHYROXINE 1 125MCG /150MCG ALTERNATIVE DAYS 0
126526431 12652643 4 C MOXONIDINE MOXONIDINE 1 AT NIGHT 0 200 UG QD
126526431 12652643 5 C NIFEDIPINE. NIFEDIPINE 1 0 20 MG QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126526431 12652643 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126526431 12652643 Acute kidney injury
126526431 12652643 Hyponatraemia

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
126526431 12652643 1 20160707 0