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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107531182 | 10753118 | 2 | F | 20160927 | 20150130 | 20160930 | PER | US-PFIZER INC-2015026356 | PFIZER | 50.00 | YR | F | Y | 0.00000 | 20160930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107531182 | 10753118 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, 2X/DAY (FOR 90 DAYS) | 20998 | 200 | MG | CAPSULE, HARD | BID | ||||||
| 107531182 | 10753118 | 2 | C | LYRICA | PREGABALIN | 1 | Oral | 100 MG, 3X/DAY | 0 | 100 | MG | TID | |||||||
| 107531182 | 10753118 | 3 | C | LORAZEPAM. | LORAZEPAM | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 4 | C | DICYCLOMINE | DICYCLOMINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 5 | C | ALBUTEROL. | ALBUTEROL | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 6 | C | PHENERGAN | PROMETHAZINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 7 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 8 | C | REMERON | MIRTAZAPINE | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 9 | C | ADVIL | IBUPROFEN | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 10 | C | LEVOTHYROXIN | LEVOTHYROXINE | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 11 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 107531182 | 10753118 | 12 | C | VITAMIN D2 | ERGOCALCIFEROL | 1 | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107531182 | 10753118 | Abdominal discomfort | |
| 107531182 | 10753118 | Hypopnoea | |
| 107531182 | 10753118 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |