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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125652501 | 12565250 | 1 | I | 20160614 | 20160617 | 20160718 | 20160718 | PER | US-PFIZER INC-2016308514 | PFIZER | 30.00 | YR | M | Y | 113.00000 | KG | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125652501 | 12565250 | 1 | PS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intramuscular | 125 MG, UNK | U | 11856 | 125 | MG | POWDER FOR SOLUTION FOR INJECTION | ||||||
| 125652501 | 12565250 | 2 | SS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | U | 11856 | POWDER FOR SOLUTION FOR INJECTION | ||||||||||
| 125652501 | 12565250 | 3 | SS | AMOXICILLIN. | AMOXICILLIN | 1 | 1000 MG, 1X/DAY (500 MG, TWO CAPSULES ONCE A DAY) | 13000 | MG | N | C16F29 | 0 | 1000 | MG | CAPSULE | QD | |||
| 125652501 | 12565250 | 4 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 125652501 | 12565250 | 5 | C | METRONIDAZOLE. | METRONIDAZOLE | 1 | 500 MG, (500 MG, EVERY 12 HOURS) | 0 | 500 | MG | |||||||||
| 125652501 | 12565250 | 6 | C | PREDNISONE. | PREDNISONE | 1 | 50 MG, UNK | 0 | 50 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125652501 | 12565250 | 1 | Urticaria |
| 125652501 | 12565250 | 2 | Hypersensitivity |
| 125652501 | 12565250 | 3 | Gastric ulcer helicobacter |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125652501 | 12565250 | Condition aggravated | |
| 125652501 | 12565250 | Hypersensitivity | |
| 125652501 | 12565250 | Product use issue | |
| 125652501 | 12565250 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 125652501 | 12565250 | 1 | 20160614 | 0 | ||
| 125652501 | 12565250 | 3 | 20160602 | 20160615 | 0 | |
| 125652501 | 12565250 | 4 | 20160614 | 0 |