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
4463188 4214084 F 4463188-2 20030802 20040915 20040930 EXP JP-ROCHE-380700 ROCHE 55 YR F Y 50 KG 20040930 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
4463188 1005252467 PS CAPECITABINE 2 UNKNOWN DOSING SCHEDULE: 3 WEEKS ADMIN/1 WEEK REST. DOSAGE WAS SUSPENDED.
4463188 1005252468 SS CAPECITABINE 2 UNKNOWN
4463188 1005252469 C AMOBAN 2 ORAL
4463188 1005252470 C MS CONTIN 1 ORAL
4463188 1005252471 C NOVAMIN 2 ORAL
4463188 1005252472 C NAUZELIN 2 ORAL
4463188 1005252473 C MAGNESIUM OXIDE 2 ORAL
4463188 1005252474 C VOLTAREN 1 OTHER
4463188 1005252475 C MAXIPIME 1 INTRAVENOUS
4463188 1005252476 C TIENAM 2 INTRAVENOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
4463188 1005252469 INSOMNIA
4463188 1005252470 CANCER PAIN
4463188 1005252473 CONSTIPATION
4463188 1005252474 CANCER PAIN
4463188 1005252475 INFECTION
4463188 1005252476 INFECTION

Outcome of event

Event ID OUTC COD
4463188 HO

Reactions reported

Event ID PT
4463188 CELLULITIS
4463188 METASTASES TO SKIN

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

Event ID RPSR COD
4463188 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4463188 1005252467 20030729 20030804 7
4463188 1005252468 20030826 20030908 14
4463188 1005252469 20030615
4463188 1005252470 20030615
4463188 1005252471 20030615
4463188 1005252472 20030615
4463188 1005252473 20030615
4463188 1005252474 20030615
4463188 1005252475 20030804 20030810 7
4463188 1005252476 20030811 20030815