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
6733697 7394372 I 6733697-1 20100429 20100512 20100520 EXP GB-BAYER-201024983GPV BAYER HEALTHCARE LLC 85 YR F Y 20100520 OT UNITED KINGDOM

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
6733697 1013720708 PS ASPIRIN 1 ORAL 021317
6733697 1013720709 SS ARTHROTEC 1 ORAL TOTAL DAILY DOSE: 150 MG
6733697 1013720710 C BISOPROLOL 2
6733697 1013720711 C IBUPROFEN 1
6733697 1013720712 C MISOPROSTOL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6733697 1013720708 PROPHYLAXIS
6733697 1013720709 PAIN
6733697 1013720710 DRUG USE FOR UNKNOWN INDICATION
6733697 1013720711 DRUG USE FOR UNKNOWN INDICATION
6733697 1013720712 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6733697 HO
6733697 LT
6733697 OT

Reactions reported

Event ID PT
6733697 ANURIA
6733697 GASTRIC ULCER HAEMORRHAGE
6733697 GASTRIC ULCER PERFORATION

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
6733697 1013720708 20100430
6733697 1013720709 20100430