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
8480325 8644631 I 8480325-3 20120401 20120621 20120630 EXP FR-AMGEN-FRASP2012039665 AMGENSAFETY 73 YR F Y 20120630 OT 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
8480325 1020135218 C CACIT D3 2 UNK
8480325 1020135219 C ALENDRONATE SODIUM 1 UNK
8480325 1020135215 C EUPRESSYL /00631801/ 2 UNK
8480325 1020135212 C METHOTREXATE 1 15 MG, UNK
8480325 1020135214 C VALSARTAN AND HYDROCHLOROTHIAZIDE 1 UNK
8480325 1020135216 C CELIPROLOL 2 UNK
8480325 1020135211 PS ENBREL 1 SUBCUTANEOUS 50 MG, UNK
8480325 1020135213 C AMLODIPINE BESYLATE 1 UNK
8480325 1020135217 C NEXIUM 1 UNK
8480325 1020135220 C ASPEGIC 1000 1 UNK
8480325 1020135221 C TRAMADOL HCL 1 UNK
8480325 1020135222 C FOLIC ACID 1 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8480325 1020135211 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
8480325 HO

Reactions reported

Event ID PT
8480325 FALL
8480325 ERYSIPELAS
8480325 HYGROMA COLLI

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
8480325 1020135211 20080101 20120521