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
127608351 12760835 1 I 201608 20160908 20160919 20160919 EXP US-ASTRAZENECA-2016SE99633 ASTRAZENECA 79.00 YR M Y 0.00000 20160920 MD SE SE

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
127608351 12760835 1 PS CANDESARTAN CANDESARTAN 1 Oral UNK U 0 TABLET
127608351 12760835 2 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown UNK U 0
127608351 12760835 3 SS FURIX FUROSEMIDE 1 Unknown UNK U 0
127608351 12760835 4 C ELIQUIS APIXABAN 1 UNK 0
127608351 12760835 5 C ALLOPURINOL. ALLOPURINOL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127608351 12760835 1 Product used for unknown indication
127608351 12760835 2 Product used for unknown indication
127608351 12760835 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127608351 12760835 OT
127608351 12760835 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127608351 12760835 Acute kidney injury
127608351 12760835 Hypotension

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
127608351 12760835 2 201607 0