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
7205768 7651892 F 7205768-7 20100816 20101221 20101231 EXP JP-PFIZER INC-2010126796 PFIZERINC 69 YR M Y 64 KG 20101231 PH JAPAN

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
7205768 1015450422 PS CELECOX 2 ORAL 200 MG, UNKNOWN/D 020998
7205768 1015450423 C DUTASTERIDE 2 ORAL UNK
7205768 1015450424 C URIEF 2 ORAL UNK
7205768 1015450425 C THYRADIN S 2 ORAL UNK
7205768 1015450426 C WARFARIN 2 UNKNOWN UNK
7205768 1015450427 C OLMETEC 2 UNK
7205768 1015450428 C MEZOLMIN 2 UNK
7205768 1015450429 C LANSOPRAZOLE 2 UNK
7205768 1015450430 C AMLODIPINE BESILATE 2 UNK
7205768 1015450431 C DOXAZOSIN MESILATE 2 UNK
7205768 1015450432 C ATENOLOL 1 UNK
7205768 1015450433 C NATRIX 2 UNK
7205768 1015450434 C TORASEMIDE 2 ORAL 100 MG, 2X/DAY

Indications of drugs used

Event ID DRUG SEQ INDI PT
7205768 1015450422 HYPOAESTHESIA
7205768 1015450434 HYPOAESTHESIA

Outcome of event

Event ID OUTC COD
7205768 DS
7205768 HO
7205768 OT

Reactions reported

Event ID PT
7205768 APHAGIA
7205768 DIARRHOEA
7205768 GASTROINTESTINAL DISORDER
7205768 HYPOALBUMINAEMIA
7205768 OEDEMA
7205768 PROTEIN-LOSING GASTROENTEROPATHY

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7205768 1015450422 20081202 20100908 646 DAY
7205768 1015450427 20080605 20100909 827 DAY
7205768 1015450428 20100904
7205768 1015450429 20080605 20100908 826 DAY
7205768 1015450430 20100908
7205768 1015450431 20100908
7205768 1015450432 20100904 20100909 6 DAY
7205768 1015450433 20100528 20100701 35 DAY
7205768 1015450434 20100904