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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118867062 | 11886706 | 2 | F | 2015 | 20160125 | 20160104 | 20160210 | PER | US-PFIZER INC-2015436858 | PFIZER | 67.00 | YR | F | Y | 60.00000 | KG | 20160210 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118867062 | 11886706 | 1 | PS | ADVIL | IBUPROFEN | 1 | 400 MG, 3X/DAY | L97476 | 18989 | 400 | MG | TABLET | TID | ||||||
118867062 | 11886706 | 2 | SS | ADVIL | IBUPROFEN | 1 | 18989 | TABLET | |||||||||||
118867062 | 11886706 | 3 | C | GABAPENTIN. | GABAPENTIN | 1 | 300 MG, DAILY (ONE AT NIGHT) | 0 | 300 | MG | CAPSULE | ||||||||
118867062 | 11886706 | 4 | C | PRAMIPEXOLE. | PRAMIPEXOLE | 1 | 0.25 MG, DAILY (ONE AT NIGHT) | 0 | .25 | MG | TABLET | ||||||||
118867062 | 11886706 | 5 | C | ASPIRIN. | ASPIRIN | 1 | 81 MG, DAILY | 0 | 81 | MG | |||||||||
118867062 | 11886706 | 6 | C | PROGESTERONE. | PROGESTERONE | 1 | 100 MG, DAILY | 0 | 100 | MG | CAPSULE | ||||||||
118867062 | 11886706 | 7 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | 88 UG, 1X/DAY | 0 | 88 | UG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
118867062 | 11886706 | 1 | Sciatica |
118867062 | 11886706 | 2 | Inflammation |
118867062 | 11886706 | 3 | Restless legs syndrome |
118867062 | 11886706 | 4 | Restless legs syndrome |
118867062 | 11886706 | 5 | Prophylaxis |
118867062 | 11886706 | 6 | Sleep disorder |
118867062 | 11886706 | 7 | Hypothyroidism |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
118867062 | 11886706 | Abdominal discomfort | |
118867062 | 11886706 | Anxiety | |
118867062 | 11886706 | Intentional product use issue | |
118867062 | 11886706 | Product use issue |
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 |
---|---|---|---|---|---|---|
118867062 | 11886706 | 1 | 201510 | 0 | ||
118867062 | 11886706 | 6 | 2013 | 0 |