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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126818901 | 12681890 | 1 | I | 20160628 | 20160816 | 20160824 | 20160824 | EXP | IT-MINISAL02-371335 | IT-MYLANLABS-2016M1034766 | MYLAN | 0.00 | Y | 0.00000 | 20160824 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126818901 | 12681890 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 25 MG, QD | U | U | 18487 | 25 | MG | TABLET | QD | ||||
| 126818901 | 12681890 | 2 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 250 MG DAILY | U | U | 18487 | 250 | MG | TABLET | QD | ||||
| 126818901 | 12681890 | 3 | C | ARANESP | DARBEPOETIN ALFA | 1 | 0 | ||||||||||||
| 126818901 | 12681890 | 4 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | 300 MG, UNK | 0 | 300 | MG | ||||||||
| 126818901 | 12681890 | 5 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | 0 | |||||||||||
| 126818901 | 12681890 | 6 | C | RANITIDINE. | RANITIDINE | 1 | Oral | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126818901 | 12681890 | 1 | Product used for unknown indication |
| 126818901 | 12681890 | 3 | Product used for unknown indication |
| 126818901 | 12681890 | 4 | Product used for unknown indication |
| 126818901 | 12681890 | 5 | Product used for unknown indication |
| 126818901 | 12681890 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126818901 | 12681890 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126818901 | 12681890 | Dehydration | |
| 126818901 | 12681890 | Orthostatic hypotension | |
| 126818901 | 12681890 | Overdose | |
| 126818901 | 12681890 | Syncope |
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 |
|---|---|---|---|---|---|---|
| 126818901 | 12681890 | 1 | 20160101 | 0 | ||
| 126818901 | 12681890 | 2 | 20160101 | 0 |