The Safety Rates Drug Report

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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
5903725 6775563 I 5903725-1 20080901 20080918 20080930 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2008-BP-14650BP B.I. PHARMACEUTICALS,INC./RIDGEFIELD 70 YR M Y 20080930 CN

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
5903725 1010521553 PS ZANTAC 150 1 ORAL 300MG NOT REPORTED 021698
5903725 1010521554 SS ZANTAC 150 1 NOT REPORTED 021698
5903725 1010521555 C SLEEPING PILLS 2
5903725 1010521556 C WELLBUTRIN 1
5903725 1010521557 C TRAZODONE HCL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5903725 1010521553 EROSIVE OESOPHAGITIS
5903725 1010521554 HIATUS HERNIA

Outcome of event

no results found

Reactions reported

Event ID PT
5903725 FATIGUE

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
5903725 1010521553 20080901