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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125941232 | 12594123 | 2 | F | 20160721 | 20160726 | 20160804 | EXP | US-AUROBINDO-AUR-APL-2016-09384 | AUROBINDO | 51.00 | YR | F | Y | 0.00000 | 20160804 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125941232 | 12594123 | 1 | PS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | U | 78619 | ||||||||||
| 125941232 | 12594123 | 2 | SS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 40 MG, DAILY | U | 78619 | 40 | MG | |||||||
| 125941232 | 12594123 | 3 | SS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 50 MG, DAILY | U | 78619 | 50 | MG | |||||||
| 125941232 | 12594123 | 4 | SS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 40 MG, DAILY | U | 78619 | 40 | MG | |||||||
| 125941232 | 12594123 | 5 | C | GABAPENTIN. | GABAPENTIN | 1 | 300 MG, QHS | U | 0 | 300 | MG | ||||||||
| 125941232 | 12594123 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | 40 MG, BID | U | 0 | 40 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125941232 | 12594123 | 1 | Depressive symptom |
| 125941232 | 12594123 | 5 | Product used for unknown indication |
| 125941232 | 12594123 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125941232 | 12594123 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125941232 | 12594123 | Abdominal pain upper | |
| 125941232 | 12594123 | Acute myocardial infarction | |
| 125941232 | 12594123 | Chest pain | |
| 125941232 | 12594123 | Diastolic dysfunction | |
| 125941232 | 12594123 | Dyspnoea | |
| 125941232 | 12594123 | Electrocardiogram ST-T segment elevation | |
| 125941232 | 12594123 | Hyperhidrosis | |
| 125941232 | 12594123 | Nausea | |
| 125941232 | 12594123 | Respiratory distress | |
| 125941232 | 12594123 | Stress cardiomyopathy | |
| 125941232 | 12594123 | Troponin increased | |
| 125941232 | 12594123 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |