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
4914423 5986151 I 4914423-5 20051212 20060206 20060216 EXP US-ABBOTT-06P-163-0324135-00 ABBOTT M Y 63.106 KG 20060216 MD UNITED STATES

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
4914423 1006944745 PS HUMIRA 1 SUBCUTANEOUS UNKNOWN
4914423 1006944746 C LEVOTHYROXINE SODIUM 1 ORAL
4914423 1006944747 C METHOTREXATE SODIUM 1 ORAL 2.5MG TABS. 8 TABS 1/DAY/WK
4914423 1006944748 C SPIREVA INHALER 2 RESPIRATORY (INHALATION)
4914423 1006944749 C SERETIDE MITE 2 RESPIRATORY (INHALATION)
4914423 1006944750 C VITAMINS 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
4914423 1006944745 RHEUMATOID ARTHRITIS
4914423 1006944746 HYPOTHYROIDISM
4914423 1006944747 RHEUMATOID ARTHRITIS
4914423 1006944748 EMPHYSEMA
4914423 1006944749 EMPHYSEMA
4914423 1006944750 VITAMIN SUPPLEMENTATION

Outcome of event

Event ID OUTC COD
4914423 HO

Reactions reported

Event ID PT
4914423 FALL
4914423 PNEUMOTHORAX TRAUMATIC
4914423 RIB FRACTURE

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
4914423 1006944745 20050201
4914423 1006944748 20040101
4914423 1006944749 20040101