Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124823542 | 12482354 | 2 | F | 20160415 | 20160818 | 20160620 | 20160826 | PER | US-APOPHARMA USA, INC.-2016AP009150 | APOTEX | 90.97 | YR | M | Y | 71.00000 | KG | 20160826 | MD | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124823542 | 12482354 | 1 | PS | ALKERAN | MELPHALAN | 1 | Oral | 12 MG, QD | 999999 | 12 | MG | ||||||||
124823542 | 12482354 | 2 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 3 | C | METOPROLOL. | METOPROLOL | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 4 | C | VITAMIN D /00107901/ | ERGOCALCIFEROL | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 5 | C | MIRALAX | POLYETHYLENE GLYCOL 3350 | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 6 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 7 | C | SENNA /00142201/ | SENNA LEAF | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 8 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 9 | C | CALCIUM | CALCIUM | 1 | Unknown | U | U | 0 | |||||||||
124823542 | 12482354 | 10 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124823542 | 12482354 | 1 | Plasma cell myeloma |
124823542 | 12482354 | 2 | Product used for unknown indication |
124823542 | 12482354 | 3 | Product used for unknown indication |
124823542 | 12482354 | 4 | Product used for unknown indication |
124823542 | 12482354 | 5 | Product used for unknown indication |
124823542 | 12482354 | 6 | Product used for unknown indication |
124823542 | 12482354 | 7 | Product used for unknown indication |
124823542 | 12482354 | 8 | Product used for unknown indication |
124823542 | 12482354 | 9 | Product used for unknown indication |
124823542 | 12482354 | 10 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124823542 | 12482354 | Diarrhoea | |
124823542 | 12482354 | Face oedema |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
124823542 | 12482354 | 1 | 20160411 | 20160415 | 0 |