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
126029164 12602916 4 F 20160829 20160728 20160914 EXP FR-PFIZER INC-2016362335 PFIZER 83.00 YR F Y 54.00000 KG 20160914 CN FR FR

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
126029164 12602916 1 PS ALDACTONE SPIRONOLACTONE 1 25 MG, 1X/DAY 12151 25 MG FILM-COATED TABLET QD
126029164 12602916 2 SS ALDACTONE SPIRONOLACTONE 1 12151 FILM-COATED TABLET
126029164 12602916 3 SS SPIRONOLACTONE. SPIRONOLACTONE 1 25 MG, UNK U 12151 25 MG FILM-COATED TABLET
126029164 12602916 4 C CARDENSIEL BISOPROLOL FUMARATE 1 Oral 7.5 MG, 1X/DAY 0 7.5 MG QD
126029164 12602916 5 C COVERSYL /00790702/ PERINDOPRIL 1 Oral 5 MG, 2X/DAY 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126029164 12602916 1 Cardiac failure
126029164 12602916 2 Congestive cardiomyopathy
126029164 12602916 3 Cardiac disorder
126029164 12602916 4 Cardiac failure
126029164 12602916 5 Cardiac failure

Outcome of event

Event ID CASEID OUTC COD
126029164 12602916 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126029164 12602916 Condition aggravated
126029164 12602916 Kidney infection
126029164 12602916 Muscle spasms
126029164 12602916 Renal failure
126029164 12602916 Renal pain

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
126029164 12602916 4 200604 0
126029164 12602916 5 200604 0