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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 115092232 | 11509223 | 2 | F | 201501 | 20160811 | 20150915 | 20160826 | EXP | US-UNICHEM LABORATORIES LIMITED-UCM201509-000802 | UNICHEM | 86.96 | YR | F | Y | 0.00000 | 20160825 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 115092232 | 11509223 | 1 | PS | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | U | 40907 | |||||||||||
| 115092232 | 11509223 | 2 | SS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 115092232 | 11509223 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 115092232 | 11509223 | Arthralgia | |
| 115092232 | 11509223 | Blood pressure increased | |
| 115092232 | 11509223 | Coagulation time shortened | |
| 115092232 | 11509223 | Dyspnoea | |
| 115092232 | 11509223 | Gastrointestinal haemorrhage | |
| 115092232 | 11509223 | Hypoacusis | |
| 115092232 | 11509223 | Wrong drug administered |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |