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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126223292 | 12622329 | 2 | F | 20160901 | 20160804 | 20160906 | PER | US-GLAXOSMITHKLINE-US2016GSK112688 | GLAXOSMITHKLINE | 0.00 | F | Y | 70.75000 | KG | 20160906 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126223292 | 12622329 | 1 | PS | WELLBUTRIN | BUPROPION HYDROCHLORIDE | 1 | U | 18644 | |||||||||||
| 126223292 | 12622329 | 2 | SS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 126223292 | 12622329 | 3 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | Oral | 0.25 MG, BID | U | 0 | .25 | MG | BID | ||||||
| 126223292 | 12622329 | 4 | C | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 50 MG, QD | U | 0 | 50 | MG | QD | ||||||
| 126223292 | 12622329 | 5 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 40 MG, QD | 0 | 40 | MG | QD | |||||||
| 126223292 | 12622329 | 6 | C | MONONESSA | ETHINYL ESTRADIOLNORGESTIMATE | 1 | U | 0 | |||||||||||
| 126223292 | 12622329 | 7 | C | ADVIL | IBUPROFEN | 1 | 800 MG, UNK | U | 0 | 800 | MG | ||||||||
| 126223292 | 12622329 | 8 | C | MOTRIN | IBUPROFEN | 1 | 800 MG, UNK | U | 0 | 800 | MG | ||||||||
| 126223292 | 12622329 | 9 | C | FIORICET | ACETAMINOPHENBUTALBITALCAFFEINE | 1 | 1 DF, PRN | U | 0 | 1 | DF | ||||||||
| 126223292 | 12622329 | 10 | C | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | Oral | 4 MG, QD | U | 0 | 4 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126223292 | 12622329 | 1 | Product used for unknown indication |
| 126223292 | 12622329 | 2 | Product used for unknown indication |
| 126223292 | 12622329 | 3 | Anxiety |
| 126223292 | 12622329 | 5 | Gastrooesophageal reflux disease |
| 126223292 | 12622329 | 10 | Nausea |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126223292 | 12622329 | Abdominal pain | |
| 126223292 | 12622329 | Abdominal pain upper | |
| 126223292 | 12622329 | Anxiety | |
| 126223292 | 12622329 | Depression | |
| 126223292 | 12622329 | Diarrhoea | |
| 126223292 | 12622329 | Drug ineffective | |
| 126223292 | 12622329 | Dysphoria | |
| 126223292 | 12622329 | Flat affect | |
| 126223292 | 12622329 | Headache | |
| 126223292 | 12622329 | Libido decreased | |
| 126223292 | 12622329 | Migraine | |
| 126223292 | 12622329 | Nausea | |
| 126223292 | 12622329 | Nervousness | |
| 126223292 | 12622329 | Product quality issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |