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
5689099 6576856 F 5689099-2 20070601 20080320 20080331 EXP TR-SANOFI-SYNTHELABO-A01200802325 SANOFI-SYNTHELABO 62 YR M Y 20080331 OT TURKEY

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
5689099 1009727664 C LEFLUNOMIDE 1 UNKNOWN 10 MG
5689099 1009727665 C LEFLUNOMIDE 1 UNKNOWN 20 MG
5689099 1009727666 C PREDNISOLONE 1 UNKNOWN 7.5 MG
5689099 1009727667 C PREDNISOLONE 1 UNKNOWN 15 MG
5689099 1009727668 C SULFASALAZINE 1 UNKNOWN 2 G
5689099 1009727669 C METHOTREXATE 1 UNKNOWN
5689099 1009727670 C METHOTREXATE 1 UNKNOWN
5689099 1009727671 PS HYDROXYCHLOROQUINE 2 UNKNOWN 009768

Indications of drugs used

Event ID DRUG SEQ INDI PT
5689099 1009727664 POLYARTHRITIS
5689099 1009727666 RHEUMATOID ARTHRITIS
5689099 1009727668 RHEUMATOID ARTHRITIS
5689099 1009727669 RHEUMATOID ARTHRITIS
5689099 1009727671 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
5689099 HO

Reactions reported

Event ID PT
5689099 HYPOGLYCAEMIA
5689099 HYPOGLYCAEMIC UNCONSCIOUSNESS

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
5689099 1009727664 20050101 20070101 2 YR
5689099 1009727665 20070101
5689099 1009727666 20050101
5689099 1009727667 20050101
5689099 1009727669 20050101
5689099 1009727671 20070401 20070601 2 MON