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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126735361 | 12673536 | 1 | I | 20140727 | 20160812 | 20160822 | 20160822 | EXP | PHHY2016CA113565 | SANDOZ | 57.00 | YR | M | Y | 0.00000 | 20160822 | OT | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126735361 | 12673536 | 1 | I | IMIPENEM+CILASTATIN SODIUM | CILASTATIN SODIUMIMIPENEM | 1 | Intravenous (not otherwise specified) | 500 MG, Q6H | 0 | 500 | MG | Q6H | |||||||
| 126735361 | 12673536 | 2 | I | AMIKACIN | AMIKACIN | 1 | Intravenous (not otherwise specified) | 900 MG, Q2H | Y | 0 | 900 | MG | Q2H | ||||||
| 126735361 | 12673536 | 3 | PS | CLARITHROMYCIN. | CLARITHROMYCIN | 1 | Oral | 500 MG, BID | 65136 | 500 | MG | BID | |||||||
| 126735361 | 12673536 | 4 | I | MEROPENEM. | MEROPENEM | 1 | Intravenous (not otherwise specified) | 1 G, Q8H | 0 | 1 | G | Q8H | |||||||
| 126735361 | 12673536 | 5 | I | WARFARIN | WARFARIN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126735361 | 12673536 | 1 | Mycobacterium abscessus infection |
| 126735361 | 12673536 | 2 | Mycobacterium abscessus infection |
| 126735361 | 12673536 | 3 | Mycobacterium abscessus infection |
| 126735361 | 12673536 | 4 | Condition aggravated |
| 126735361 | 12673536 | 5 | Anticoagulant therapy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126735361 | 12673536 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126735361 | 12673536 | Drug interaction | |
| 126735361 | 12673536 | Gastrointestinal haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 126735361 | 12673536 | 3 | 20140717 | 0 |