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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125595081 | 12559508 | 1 | I | 20160620 | 20160621 | 20160715 | 20160715 | PER | US-PFIZER INC-2016311937 | PFIZER | 47.00 | YR | F | Y | 54.43000 | KG | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125595081 | 12559508 | 1 | PS | ADVIL PM | DIPHENHYDRAMINE CITRATEIBUPROFEN | 1 | Y | 21393 | CAPSULE | ||||||||||
| 125595081 | 12559508 | 2 | SS | ALEVE | NAPROXEN SODIUM | 1 | Oral | 2 DF, UNK (TOOK TWO TABLETS, ONE TIME DOSE) | U | 0 | 2 | DF | TABLET | ||||||
| 125595081 | 12559508 | 3 | C | HYDROCODONE | HYDROCODONE | 1 | Oral | 10/325 MO, TABLET, EVERY 6 HOURS AS NEEDED | 0 | TABLET | |||||||||
| 125595081 | 12559508 | 4 | C | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Oral | 10 MG, 3X/DAY (10MG, THREE TIMES A DAY, TABLET) | 0 | 10 | MG | TABLET | TID | ||||||
| 125595081 | 12559508 | 5 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 20 MG, 2X/DAY(20MG, TWICE A DAY, CAPSULE) | 0 | 20 | MG | CAPSULE | BID | ||||||
| 125595081 | 12559508 | 6 | C | MIRTAZAPINE. | MIRTAZAPINE | 1 | Oral | 15 MG, 1X/DAY(15MG, ONCE AT NIGHT, TABLET) | 0 | 15 | MG | TABLET | QD | ||||||
| 125595081 | 12559508 | 7 | C | HALDOL | HALOPERIDOL | 1 | Oral | 20 MG, 3X/DAY(20MG, THREE TIMES A DAY, TABLET) | 0 | 20 | MG | TABLET | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125595081 | 12559508 | 2 | Arthritis |
| 125595081 | 12559508 | 3 | Pain |
| 125595081 | 12559508 | 4 | Depression |
| 125595081 | 12559508 | 5 | Dyspepsia |
| 125595081 | 12559508 | 6 | Sleep disorder |
| 125595081 | 12559508 | 7 | Depression |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125595081 | 12559508 | Contusion | |
| 125595081 | 12559508 | Pruritus | |
| 125595081 | 12559508 | Urticaria | |
| 125595081 | 12559508 | Wrong drug administered |
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 |
|---|---|---|---|---|---|---|
| 125595081 | 12559508 | 2 | 2012 | 0 | ||
| 125595081 | 12559508 | 3 | 2014 | 0 | ||
| 125595081 | 12559508 | 4 | 2016 | 0 | ||
| 125595081 | 12559508 | 5 | 2014 | 0 | ||
| 125595081 | 12559508 | 6 | 2016 | 0 | ||
| 125595081 | 12559508 | 7 | 2016 | 201606 | 0 |