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
5195456 6206063 I 5195456-3 20060625 20061221 20061230 EXP CO-ABBOTT-06P-036-0354112-00 ABBOTT 37 YR F Y 55 KG 20061230 MD 20060718 COLOMBIA

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
5195456 1007999526 PS AVONEX 1 INTRAMUSCULAR UNKNOWN
5195456 1007999527 SS AZATHIOPRINE 1 ORAL
5195456 1007999528 C GABAPENTIN 1 ORAL
5195456 1007999529 C PREGABALINE 2 ORAL
5195456 1007999530 C CORTISONE PULSE THERAPY 2 INTRAVENOUS PULSE THERAPY
5195456 1007999531 C CALCIUM 2 ORAL
5195456 1007999532 C PREDNISOLONE 1 ORAL
5195456 1007999533 C ALENDRONATE SODIUM 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5195456 1007999526 MULTIPLE SCLEROSIS
5195456 1007999527 MULTIPLE SCLEROSIS
5195456 1007999528 NEURALGIA
5195456 1007999529 NEURALGIA
5195456 1007999530 MULTIPLE SCLEROSIS RELAPSE
5195456 1007999531 OSTEOPOROSIS
5195456 1007999532 MULTIPLE SCLEROSIS
5195456 1007999533 OSTEOPOROSIS

Outcome of event

Event ID OUTC COD
5195456 DE
5195456 HO
5195456 LT

Reactions reported

Event ID PT
5195456 SEPSIS
5195456 URINARY TRACT INFECTION

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
5195456 1007999526 20010101 20060718
5195456 1007999527 20060514 20060702
5195456 1007999528 20050501 20060501
5195456 1007999529 20050501 20060501
5195456 1007999531 20040101 20060501
5195456 1007999533 20050501 20060501