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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125845791 | 12584579 | 1 | I | 20160721 | 20160722 | 20160722 | EXP | GB-MHRA-MIDB-14367D93-B290 | GB-FRESENIUS KABI-FK201604706 | FRESENIUS KABI | 47.00 | YR | F | Y | 0.00000 | 20160722 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125845791 | 12584579 | 1 | PS | FUROSEMIDE (MANUFACTURER UNKNOWN) | FUROSEMIDE | 1 | Oral | U | UNKNOWN | 18902 | 80 | MG | UNKNOWN | BID | |||||
| 125845791 | 12584579 | 2 | SS | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Oral | 0 | |||||||||||
| 125845791 | 12584579 | 3 | SS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 0 | 75 | MG | QD | ||||||||
| 125845791 | 12584579 | 4 | SS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Unknown | 0 | 37.5 | MG | |||||||||
| 125845791 | 12584579 | 5 | C | CETIRIZINE | CETIRIZINE HYDROCHLORIDE | 1 | Oral | 0 | 10 | MG | QD | ||||||||
| 125845791 | 12584579 | 6 | C | CHLORHEXIDINE GLUCONATE. | CHLORHEXIDINE GLUCONATE | 1 | Topical | 0 | |||||||||||
| 125845791 | 12584579 | 7 | C | CLOTRIMAZOLE. | CLOTRIMAZOLE | 1 | Topical | 0 | 1 | DF | BID | ||||||||
| 125845791 | 12584579 | 8 | C | DIPROBASE | CHLOROCRESOL | 1 | Topical | 0 | |||||||||||
| 125845791 | 12584579 | 9 | C | NYSTATIN. | NYSTATIN | 1 | Oral | 0 | 1 | ML | QID | ||||||||
| 125845791 | 12584579 | 10 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 0 | 20 | MG | QD | ||||||||
| 125845791 | 12584579 | 11 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Oral | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125845791 | 12584579 | 1 | Product used for unknown indication |
| 125845791 | 12584579 | 2 | Product used for unknown indication |
| 125845791 | 12584579 | 3 | Product used for unknown indication |
| 125845791 | 12584579 | 5 | Product used for unknown indication |
| 125845791 | 12584579 | 6 | Product used for unknown indication |
| 125845791 | 12584579 | 7 | Product used for unknown indication |
| 125845791 | 12584579 | 8 | Product used for unknown indication |
| 125845791 | 12584579 | 9 | Product used for unknown indication |
| 125845791 | 12584579 | 10 | Product used for unknown indication |
| 125845791 | 12584579 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125845791 | 12584579 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125845791 | 12584579 | Acute kidney injury | |
| 125845791 | 12584579 | Chest pain | |
| 125845791 | 12584579 | Diarrhoea | |
| 125845791 | 12584579 | Dyspnoea | |
| 125845791 | 12584579 | Loss of consciousness |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |