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
4412692 4191388 I 4412692-1 20040308 20040317 20040630 PER 04P-163-0253899-00 PPD PHARMACOVIGILANCE 45 YR F N 250 LBS 20040317 MD

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
4412692 1005066469 PS HUMIRA 1 SUBCUTANEOUS 40 MG, 1 IN 1 WK, SUBCUTANEOUS D D
4412692 1005115908 SS METHOTREXATE 1 INTRAMUSCULAR 25 MG, 1 IN 1 WK, INTRAMUSCULAR D D
4412692 1005115909 C PREDNISONE 1
4412692 1005115910 C HYDROXYCHLOROQUINE PHOSPHATE 2
4412692 1005115911 C FOLIC ACID 1
4412692 1005115912 C FOLINIC ACID 2
4412692 1005115913 C FENTANYL 1
4412692 1005115914 C GLIPIZIDE 1
4412692 1005115915 C MESALAMINE 1
4412692 1005115916 C BUDESONIDE 2
4412692 1005115917 C LISINOPRIL 1
4412692 1005115918 C OMEPRAZOLE 1
4412692 1005115919 C RANITIDINE HYDROCHLORIDE 1
4412692 1005115920 C VICODIN 1
4412692 1005115921 C IRON 2
4412692 1005115922 C DILTIAZEM HYDROCHLORIDE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4412692 1005066469 RHEUMATOID ARTHRITIS
4412692 1005115908 RHEUMATOID ARTHRITIS

Outcome of event

no results found

Reactions reported

Event ID PT
4412692 ARTHRITIS
4412692 HERPES ZOSTER

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4412692 CR
4412692 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4412692 1005066469 20030101