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
126063291 12606329 1 I 2015 20160706 20160729 20160729 PER US-PFIZER INC-2016334607 PFIZER 50.00 YR M Y 0.00000 20160729 CN US US

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
126063291 12606329 1 PS GABAPENTIN. GABAPENTIN 1 Oral 300 MG, THREE TIMES A DAY OR TWICE A DAY Y 20235 300 MG CAPSULE, HARD
126063291 12606329 2 C SPIRONOLACTONE. SPIRONOLACTONE 1 UNK 0
126063291 12606329 3 C COREG CARVEDILOL 1 Oral 12.5 MG, 2X/DAY 0 12.5 MG TABLET BID
126063291 12606329 4 C COREG CARVEDILOL 1 0 TABLET
126063291 12606329 5 C FUROSEMIDE. FUROSEMIDE 1 Oral 80 MG, 2X/DAY 0 80 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126063291 12606329 1 Neuropathy peripheral
126063291 12606329 2 Blood pressure abnormal
126063291 12606329 3 Blood pressure abnormal
126063291 12606329 4 Cardiac failure
126063291 12606329 5 Diuretic therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126063291 12606329 Condition aggravated
126063291 12606329 Drug ineffective for unapproved indication
126063291 12606329 Urinary incontinence

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
126063291 12606329 1 2015 201511 0
126063291 12606329 2 2013 0
126063291 12606329 3 2013 0
126063291 12606329 5 2013 0