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 |