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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116461562 | 11646156 | 2 | F | 20150928 | 20160707 | 20151020 | 20160708 | EXP | GB-AUROBINDO-AUR-APL-2015-09364 | AUROBINDO | 82.00 | YR | M | Y | 59.00000 | KG | 20160708 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116461562 | 11646156 | 1 | PS | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Oral | 75 MG, ONCE A DAY | Y | U | 90540 | 75 | MG | QD | |||||
| 116461562 | 11646156 | 2 | C | IRBESARTAN. | IRBESARTAN | 1 | Unknown | U | 0 | ||||||||||
| 116461562 | 11646156 | 3 | C | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | U | 0 | ||||||||||
| 116461562 | 11646156 | 4 | C | RANITIDINE. | RANITIDINE | 1 | Unknown | U | 0 | ||||||||||
| 116461562 | 11646156 | 5 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Unknown | 250 | U | 0 | |||||||||
| 116461562 | 11646156 | 6 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 116461562 | 11646156 | 1 | Product used for unknown indication |
| 116461562 | 11646156 | 2 | Product used for unknown indication |
| 116461562 | 11646156 | 3 | Product used for unknown indication |
| 116461562 | 11646156 | 4 | Product used for unknown indication |
| 116461562 | 11646156 | 5 | Product used for unknown indication |
| 116461562 | 11646156 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 116461562 | 11646156 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116461562 | 11646156 | Gastrointestinal ulcer | |
| 116461562 | 11646156 | Haemoglobin decreased | |
| 116461562 | 11646156 | Upper 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 |
|---|---|---|---|---|---|---|
| 116461562 | 11646156 | 1 | 20150927 | 0 |