The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
4390411 4165153 F 1 4390411-5 20040616 20040630 EXP 2004039501 PFIZER INC 72 YR F N 163 LBS 20040628

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
4390411 1004989430 PS TIKOSYN 1 ORAL 1000 MCG (500 MCG, 2 IN 1 D), ORAL Y D 20931
4390411 1005004273 C DIGOXIN 1
4390411 1005004274 C LANSOPRAZOLE 1
4390411 1005004277 C TOLTERODINE L-TARTRATE (TOLTERODINE L-TARTRATE) 2
4390411 1005004279 C LISINOPRIL 1
4390411 1005004280 C BRIMONIDINE TARTRATE (BRIMONIDINE TARTRATE) 2
4390411 1005004281 C LATANOPROST 1
4390411 1005004282 C ACETAZOLAMIDE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4390411 1004989430 ATRIAL FIBRILLATION

Outcome of event

Event ID OUTC COD
4390411 HO
4390411 OT

Reactions reported

Event ID PT
4390411 ATRIAL FIBRILLATION
4390411 CATARACT
4390411 CONDITION AGGRAVATED
4390411 ELECTROCARDIOGRAM QT PROLONGED
4390411 HAEMORRHAGE
4390411 LABILE HYPERTENSION
4390411 RECTAL POLYP
4390411 SINUS BRADYCARDIA

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4390411 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4390411 1004989430 20020101