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
6528854 6647735 F 6528854-3 20040901 20091223 20100106 EXP GB-BAUSCH-2006BL004483 BAUSCH + LOMB INCORPORATED 68 YR F Y 58 KG 20100106 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
6528854 1012907830 PS PREDNISOLONE 1 ORAL 40070
6528854 1012907831 SS ENBREL 1
6528854 1012907832 SS REMICADE 1 INTRAVENOUS
6528854 1012907833 SS FOSAMAX 1 ORAL 40070
6528854 1012907834 C CO-DYDRAMOL 2 ORAL
6528854 1012907835 C LISINOPRIL 1 ORAL 40070
6528854 1012907836 C ZOPICLONE 2 ORAL
6528854 1012907837 C AMITRIPTYLINE 2
6528854 1012907838 C PLAQUENIL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6528854 1012907830 RHEUMATOID ARTHRITIS
6528854 1012907831 RHEUMATOID ARTHRITIS
6528854 1012907832 RHEUMATOID ARTHRITIS
6528854 1012907834 ARTHRALGIA
6528854 1012907835 HYPERTENSION
6528854 1012907836 SLEEP DISORDER

Outcome of event

Event ID OUTC COD
6528854 HO
6528854 OT

Reactions reported

Event ID PT
6528854 BASAL CELL CARCINOMA
6528854 ECZEMA

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
6528854 1012907830 19960101
6528854 1012907831 20040712 20041101
6528854 1012907832 20020513 20040305
6528854 1012907833 20020101