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
126698282 12669828 2 F 20160822 20160819 20160826 EXP GB-MHRA-EYC 00143559 GB-PFIZER INC-2016388020 PFIZER 65.00 YR M Y 0.00000 20160826 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
126698282 12669828 1 PS SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 100 MG, 1X/DAY Y 12151 100 MG QD
126698282 12669828 2 C ATORVASTATIN ATORVASTATIN 1 UNK 0
126698282 12669828 3 C ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) UNK 0
126698282 12669828 4 C BISOPROLOL BISOPROLOL 1 UNK 0
126698282 12669828 5 C DOXAZOSIN DOXAZOSINDOXAZOSIN MESYLATE 1 UNK 0
126698282 12669828 6 C FINASTERIDE. FINASTERIDE 1 UNK 0
126698282 12669828 7 C FUROSEMIDE. FUROSEMIDE 1 UNK 0
126698282 12669828 8 C SALBUTAMOL ALBUTEROL 1 Respiratory (inhalation) UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126698282 12669828 1 Cardiac failure chronic

Outcome of event

Event ID CASEID OUTC COD
126698282 12669828 HO
126698282 12669828 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126698282 12669828 Accidental overdose
126698282 12669828 Acute kidney injury
126698282 12669828 Hyperkalaemia

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
126698282 12669828 1 201607 0