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
4465977 5664780 I 4465977-7 20040920 20040930 EXP STA-AE-04-MTX-426 STADA PHARMACEUTICALS, INC. 63 YR F N 20040920 OT

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
4465977 1005265064 PS METHOTREXATE 1 ORAL 7.5 MG, ORAL D D 8085
4465977 1005287330 C ASPIRIN 1
4465977 1005287331 C FUROSEMIDE 1
4465977 1005287332 C METOPROLOL TARTRATE 1
4465977 1005287334 C SIMVASTATIN 1
4465977 1005287335 C RAMIPRIL 1
4465977 1005287336 C ROFECOXIB 1
4465977 1005287337 C ACYCLOVIR 1
4465977 1005287338 C AMOXICILLIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4465977 1005265064 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
4465977 DE

Reactions reported

Event ID PT
4465977 CARDIAC FAILURE

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

Event ID RPSR COD
4465977 DT
4465977 FGN
4465977 HP
4465977 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4465977 1005265064 20040506