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
5477131 6118682 F 5477131-0 20060710 20071002 20071004 EXP HQWYE252509AUG06 WYETH PHARMACEUTICALS INC. 53 YR M Y 20071004 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
5477131 1009006302 PS PROPRANOLOL HCL 1 ORAL 18553
5477131 1009006303 SS MORPHINE 1 ORAL NOT PROVIDED
5477131 1009006304 SS STABLON 2 ORAL
5477131 1009006305 SS ALDACTONE 1 ORAL
5477131 1009006306 C CLAMOXYL 2 INTRAVENOUS
5477131 1009006307 C LANTUS 1 UNKNOWN
5477131 1009006308 C DUPHALAC 1 UNKNOWN
5477131 1009006309 C VITAMIN B1 AND B6 2 UNKNOWN
5477131 1009006310 C NOVORAPID 2 UNKNOWN
5477131 1009006311 SS PENTOXIFYLLINE 1 ORAL
5477131 1009006312 SS ACETAMINOPHEN W/ CODEINE 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5477131 1009006304 DEPRESSION
5477131 1009006311 CIRRHOSIS ALCOHOLIC

Outcome of event

Event ID OUTC COD
5477131 HO

Reactions reported

Event ID PT
5477131 HEPATIC ENCEPHALOPATHY
5477131 INFECTION

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
5477131 1009006303 20060705 20060710 6 DAY
5477131 1009006308 20060701
5477131 1009006311 20060106 20060713 189 DAY
5477131 1009006312 20060705 20060710 6 DAY