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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125414111 | 12541411 | 1 | I | 20160627 | 20160708 | 20160708 | EXP | US-PERRIGO-16US017521 | PERRIGO | 56.00 | YR | F | Y | 0.00000 | 20160708 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125414111 | 12541411 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | UP TO 3200 MG, QD | Y | UNKNOWN | 72096 | 3200 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125414111 | 12541411 | 1 | Headache |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125414111 | 12541411 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125414111 | 12541411 | Abdominal pain | |
| 125414111 | 12541411 | Acute kidney injury | |
| 125414111 | 12541411 | Blood lactate dehydrogenase increased | |
| 125414111 | 12541411 | Evans syndrome | |
| 125414111 | 12541411 | Headache | |
| 125414111 | 12541411 | Nausea | |
| 125414111 | 12541411 | Red blood cell schistocytes present | |
| 125414111 | 12541411 | Tubulointerstitial nephritis | |
| 125414111 | 12541411 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |