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
5472364 6395482 F 5472364-1 20030101 20070919 20070930 EXP CA-SHR-CA-2007-031016 BERLEX 43 YR F Y 84 KG 20070928 CANADA

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
5472364 1008989676 PS BETASERON 1 SUBCUTANEOUS 8 MIU, EVERY 2D
5472364 1008989677 C BACLOFEN 1 ORAL
5472364 1008989678 C GABAPENTIN 1 ORAL
5472364 1008989679 C LORAZEPAM 1 ORAL
5472364 1008989680 C NADOLOL 1 ORAL
5472364 1008989681 C OXYCOCET 2 ORAL
5472364 1008989682 C OXYCODONE HCL 1 ORAL
5472364 1008989683 C HYDROCHLOROTHIAZIDE 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5472364 1008989676 RELAPSING-REMITTING MULTIPLE SCLEROSIS
5472364 1008989679 SEDATIVE THERAPY
5472364 1008989680 HYPERTENSION
5472364 1008989681 PAIN
5472364 1008989682 PAIN
5472364 1008989683 HYPERTENSION

Outcome of event

Event ID OUTC COD
5472364 HO
5472364 OT

Reactions reported

Event ID PT
5472364 ACCIDENT
5472364 HIP SURGERY
5472364 HOT FLUSH
5472364 INJECTION SITE ERYTHEMA
5472364 LIMB INJURY
5472364 URTICARIA

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
5472364 1008989676 20010607