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
5126537 6077716 F 1 5126537-8 20060602 20060928 20061010 EXP 163-C5013-06060434 CELGENE CORPORATION 61 YR F N 81.6 KG 20060928 MD 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
5126537 1007754403 PS REVLIMID 1 ORAL 25 MG, DAILY X21 DAYS, ORAL Y D 21880
5126537 1007772033 SS DEXAMETHASONE TAB 1 ORAL ORAL
5126537 1007772035 C CALTRATE 600 PLUS VITAMIN D (CALTRATE PLUS) 2
5126537 1007772036 C NEURONTIN 1
5126537 1007772038 C LOPRESSOR (METOPROL TARTRATE) 2
5126537 1007772039 C ACYCLOVIR 1
5126537 1007772040 C PAROXETINE HCL 1
5126537 1007772041 C LIPITOR 1
5126537 1007772042 C LEVOXYL 1
5126537 1007772043 C ALLOPURINOL 1
5126537 1007772044 C FLUCONAZOLE 1
5126537 1007772045 C COZAAR 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5126537 1007754403 MULTIPLE MYELOMA
5126537 1007772033 MULTIPLE MYELOMA

Outcome of event

Event ID OUTC COD
5126537 HO

Reactions reported

Event ID PT
5126537 ALANINE AMINOTRANSFERASE INCREASED
5126537 ASPARTATE AMINOTRANSFERASE INCREASED
5126537 BACK PAIN
5126537 BLOOD ALBUMIN DECREASED
5126537 BLOOD AMYLASE INCREASED
5126537 BLOOD CHLORIDE INCREASED
5126537 BLOOD CREATININE INCREASED
5126537 BLOOD GLUCOSE INCREASED
5126537 BLOOD UREA INCREASED
5126537 CONFUSIONAL STATE
5126537 ECCHYMOSIS
5126537 EYE DISORDER
5126537 FALL
5126537 LUNG CONSOLIDATION
5126537 MENTAL STATUS CHANGES
5126537 MUSCLE SPASMS
5126537 OXYGEN SATURATION DECREASED
5126537 PLATELET COUNT DECREASED
5126537 PNEUMONIA
5126537 PROTEIN TOTAL DECREASED
5126537 PROTEIN URINE
5126537 RECTAL HAEMORRHAGE
5126537 WHITE BLOOD CELL COUNT DECREASED

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

Event ID RPSR COD
5126537 HP
5126537 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5126537 1007754403 20060518 20060601
5126537 1007772033 20060518 20060601