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
4746869 5862326 F 4746869-2 20001201 20020422 20050817 EXP SE-AMGEN-02040719 AMGEN F Y 20050817 SWEDEN

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
4746869 1006328792 PS ENBREL 1 SUBCUTANEOUS UNKNOWN
4746869 1006328793 SS ENBREL 1 UNKNOWN
4746869 1006328794 C EFFORTIL 2
4746869 1006328795 C PREDNISOLONE 1
4746869 1006328796 C METHENAMINE HIPPURATE 1
4746869 1006328797 C OMEPRAZOLE MAGNESIUM 2
4746869 1006328798 C METHOTREXATE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4746869 1006328792 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
4746869 HO

Reactions reported

Event ID PT
4746869 CUTANEOUS TUBERCULOSIS
4746869 IMPAIRED HEALING
4746869 SKIN ULCER
4746869 STAPHYLOCOCCAL INFECTION
4746869 WOUND INFECTION STAPHYLOCOCCAL

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
4746869 1006328792 19990801 20010601