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
4914165 5966425 F 4914165-6 20050704 20050706 20060216 EXP ZA-BRISTOL-MYERS SQUIBB COMPANY-13026596 BRISTOL-MYERS SQUIBB COMPANY 62 YR F Y 20060216 CN 20050715 SOUTH AFRICA

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
4914165 1006944292 PS ABATACEPT 2 INTRAVENOUS
4914165 1006944293 SS METHOTREXATE 1 ORAL
4914165 1006944294 C RISEDRONATE SODIUM 1 ORAL
4914165 1006944295 C PREDNISONE 1 ORAL
4914165 1006944296 C ACETAMINOPHEN 1 ORAL
4914165 1006944297 C FOLIC ACID 1 ORAL
4914165 1006944298 C CALTRATE VITAMINE D3 2 ORAL
4914165 1006944299 C TEMAZEPAM 1 ORAL
4914165 1006944300 C MELOXICAM 1 ORAL
4914165 1006944301 C PREGAMAL 2 ORAL
4914165 1006944302 C DOXYFENE 2 ORAL
4914165 1006944303 C DEXTROPROPO+APAP+PEMOLINE+GLUTAMINE 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
4914165 1006944292 RHEUMATOID ARTHRITIS
4914165 1006944293 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
4914165 DE
4914165 HO
4914165 LT

Reactions reported

Event ID PT
4914165 HYPOVOLAEMIC SHOCK
4914165 PNEUMONIA
4914165 RENAL FAILURE ACUTE
4914165 RETROPERITONEAL HAEMORRHAGE
4914165 SEPTIC SHOCK
4914165 SINUSITIS

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
4914165 1006944292 20040521 20050620
4914165 1006944293 20030109
4914165 1006944294 20030109
4914165 1006944295 20030210
4914165 1006944296 20030109
4914165 1006944297 20030109
4914165 1006944298 20030109
4914165 1006944299 20041105
4914165 1006944300 20050518
4914165 1006944301 20040903
4914165 1006944302 20031031
4914165 1006944303 20030617