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
126305062 12630506 2 F 201604 20160805 20160808 20160822 PER US-PFIZER INC-2016344546 PFIZER 90.00 YR F Y 55.79000 KG 20160822 MD 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
126305062 12630506 1 PS TOVIAZ FESOTERODINE FUMARATE 1 Oral 4 MG, 1X/DAY 22030 4 MG MODIFIED-RELEASE TABLET QD
126305062 12630506 2 C AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 UNK 0
126305062 12630506 3 C AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 1 DF, DAILY (ONE DAILY) 0 1 DF
126305062 12630506 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 112 UG, DAILY (112MCG, ONE A DAY) 0 112 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126305062 12630506 1 Hypertonic bladder
126305062 12630506 2 Blood pressure abnormal
126305062 12630506 4 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126305062 12630506 Condition aggravated
126305062 12630506 Dizziness
126305062 12630506 Joint swelling

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
126305062 12630506 1 201604 0
126305062 12630506 3 201603 0