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
4634579 5723153 F 1 4634579-1 20040903 20050404 20050411 EXP 2005-01-0302 SCHERING-PLOUGH CORPORATION 63 YR F N 80 KG 20050404 MD FRANCE

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
4634579 1005875200 PS VIRAFERONPEG 1 SUBCUTANEOUS 120MG QW SC SUBCUTANEOUS Y D
4634579 1005897071 SS REBETOL 1 ORAL 1G WF PO ORAL Y D
4634579 1005897074 C SEROPRAM (CITALOPRAM HBR) 2
4634579 1005897075 C TRANXENE 1
4634579 1005897077 C TERCIAN 2
4634579 1005897079 C LEVOTHYROX 2
4634579 1005897081 C PROPRANOLOL HYDROCHLORIDE 1
4634579 1005897082 C PANTOPRAZOL 2
4634579 1005897083 C EVISTA 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4634579 1005875200 HEPATITIS C
4634579 1005897071 HEPATITIS C

Outcome of event

Event ID OUTC COD
4634579 OT

Reactions reported

Event ID PT
4634579 DEMYELINATION
4634579 POLYNEUROPATHY

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

Event ID RPSR COD
4634579 FGN
4634579 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4634579 1005875200 20040628 20040903
4634579 1005897071 20040628 20040903