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
5472352 6431117 F 5472352-5 20070101 20070919 20070930 EXP US-SHR-US-2007-023206 BERLEX 49 YR M Y 20070928 CN 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
5472352 1008989649 PS BETASERON 1 SUBCUTANEOUS 8 MIU, EVERY 2D WA6215A
5472352 1008989650 C ARICEPT 1
5472352 1008989651 C BACLOFEN 1
5472352 1008989652 C PAXIL 1
5472352 1008989653 C ULTRAM 1
5472352 1008989654 C ATIVAN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5472352 1008989649 MULTIPLE SCLEROSIS
5472352 1008989652 DEPRESSION
5472352 1008989653 PAIN
5472352 1008989654 ANXIETY

Outcome of event

Event ID OUTC COD
5472352 OT

Reactions reported

Event ID PT
5472352 HEPATIC CIRRHOSIS
5472352 INTERVERTEBRAL DISC PROTRUSION
5472352 MULTIPLE SCLEROSIS
5472352 POLYPECTOMY
5472352 UMBILICAL HERNIA

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
5472352 1008989649 20030314 20070819 1619 DAY