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
6255598 6735804 F 3 6255598-8 20090101 20090618 20090701 EXP 237135J08USA EMD SERONO, INC. 44 YR F N 20090622 OT 20090606 UNITED STATES

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
6255598 1011834735 PS REBIF 1 SUBCUTANEOUS 44 MCG, 3 IN 1 WEEKS, SUBCUTANEOUS D D
6255598 1011872510 SS CHEMOTHERAPY (OTHER CHEMOTHERAPEUTICS) 2 N D
6255598 1011872511 C MAXZIDE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6255598 1011834735 MULTIPLE SCLEROSIS
6255598 1011872510 COLON CANCER

Outcome of event

Event ID OUTC COD
6255598 DE
6255598 HO
6255598 OT

Reactions reported

Event ID PT
6255598 BLOOD PRESSURE DECREASED
6255598 CHEST PAIN
6255598 COLON CANCER STAGE IV
6255598 DECREASED APPETITE
6255598 DEHYDRATION
6255598 DIALYSIS
6255598 GASTROOESOPHAGEAL REFLUX DISEASE
6255598 INSOMNIA
6255598 MALAISE
6255598 NAUSEA
6255598 PAIN
6255598 RENAL FAILURE ACUTE
6255598 URINARY TRACT INFECTION
6255598 UTERINE LEIOMYOMA
6255598 VOMITING
6255598 WOUND DEHISCENCE

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

Event ID RPSR COD
6255598 CSM
6255598 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6255598 1011834735 20061212 20090605
6255598 1011872510 20080716 20090501