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
4331049 4122440 I 4331049-5 20040314 20040318 20040331 EXP 2004018942 WWS PFIZER INC 68 YR F N 150 LBS 20040330

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
4331049 1004758795 PS ZOLOFT 1 ORAL 25 MG (DAILY), ORAL Y D 19839
4331049 1004773535 SS NITROGLYCERIN 1 Y N
4331049 1004773537 SS ACETYLSALICYLIC ACID SRT 1 Y N
4331049 1004773538 SS EZETIMIBE (EZETIMIBE) 2 Y N
4331049 1004773540 SS METOPROLOL TARTRATE 1 Y N
4331049 1004773542 SS WARFARIN SODIUM 1 Y N

Indications of drugs used

Event ID DRUG SEQ INDI PT
4331049 1004758795 DEPRESSION
4331049 1004773535 ANGINA PECTORIS
4331049 1004773537 CORONARY ARTERY DISEASE
4331049 1004773538 BLOOD CHOLESTEROL INCREASED
4331049 1004773540 CARDIAC VALVE DISEASE
4331049 1004773540 EXTRASYSTOLES
4331049 1004773540 TACHYCARDIA
4331049 1004773542 PULMONARY EMBOLISM

Outcome of event

Event ID OUTC COD
4331049 HO

Reactions reported

Event ID PT
4331049 BLOOD PRESSURE INCREASED
4331049 BURNING SENSATION
4331049 CEREBROVASCULAR ACCIDENT
4331049 CONFUSIONAL STATE
4331049 DRUG INTERACTION
4331049 HYPOAESTHESIA

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

Event ID RPSR COD
4331049 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4331049 1004758795 20040313 20040313