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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125695461 | 12569546 | 1 | I | 20160715 | 20160719 | 20160719 | EXP | US-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00323 | SCIEGEN | 51.00 | YR | F | Y | 0.00000 | 20160719 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125695461 | 12569546 | 1 | PS | Fluoxetine Capsules, USP | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 40 MG, QD | Y | U | 204597 | 40 | MG | CAPSULE | |||||
| 125695461 | 12569546 | 2 | SS | Fluoxetine Capsules, USP | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 50 MG, QD | Y | U | 204597 | 50 | MG | CAPSULE | |||||
| 125695461 | 12569546 | 3 | SS | Fluoxetine Capsules, USP | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 40 MG, QD | Y | U | 204597 | 40 | MG | CAPSULE | |||||
| 125695461 | 12569546 | 4 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | 40 MG, BID | 0 | 40 | MG | ||||||||
| 125695461 | 12569546 | 5 | SS | GABAPENTIN. | GABAPENTIN | 1 | 300 MG, UNK | 0 | 300 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125695461 | 12569546 | 1 | Depressive symptom |
| 125695461 | 12569546 | 4 | Product used for unknown indication |
| 125695461 | 12569546 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125695461 | 12569546 | OT |
| 125695461 | 12569546 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125695461 | 12569546 | Abdominal pain upper | |
| 125695461 | 12569546 | Chest pain | |
| 125695461 | 12569546 | Dyspnoea | |
| 125695461 | 12569546 | Hyperhidrosis | |
| 125695461 | 12569546 | Nausea | |
| 125695461 | 12569546 | Stress cardiomyopathy | |
| 125695461 | 12569546 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |