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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127804031 | 12780403 | 1 | I | 20130806 | 20160912 | 20160926 | 20160926 | EXP | US-VALIDUS PHARMACEUTICALS LLC-US-2016VAL002686 | VALIDUS | 64.00 | YR | F | Y | 0.00000 | 20160926 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127804031 | 12780403 | 1 | PS | LASIX | FUROSEMIDE | 1 | Oral | 20 MG, QD | Y | 16273 | 20 | MG | TABLET | ||||||
127804031 | 12780403 | 2 | SS | INDOMETHACIN /00003801/ | INDOMETHACIN | 1 | Oral | 50 MG, BID | Y | 0 | 50 | MG | |||||||
127804031 | 12780403 | 3 | SS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, QD | Y | 0 | 200 | MG | |||||||
127804031 | 12780403 | 4 | SS | CELECOXIB. | CELECOXIB | 1 | Oral | UNK, TID | D | 0 | |||||||||
127804031 | 12780403 | 5 | SS | CELECOXIB. | CELECOXIB | 1 | D | 0 | |||||||||||
127804031 | 12780403 | 6 | SS | IBUPROFEN. | IBUPROFEN | 1 | Oral | UNK, TID | D | 0 | |||||||||
127804031 | 12780403 | 7 | SS | IBUPROFEN. | IBUPROFEN | 1 | D | 0 | |||||||||||
127804031 | 12780403 | 8 | SS | NAPROXEN. | NAPROXEN | 1 | Oral | UNK, TID | D | 0 | |||||||||
127804031 | 12780403 | 9 | SS | NAPROXEN. | NAPROXEN | 1 | D | 0 | |||||||||||
127804031 | 12780403 | 10 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 11 | C | COREG | CARVEDILOL | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 12 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 13 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 14 | C | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 15 | C | NOVOLOG | INSULIN ASPART | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 16 | C | TRAMADOL. | TRAMADOL | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 17 | C | ZANAFLEX | TIZANIDINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 18 | C | COLCHICINE. | COLCHICINE | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 19 | C | PRAVASTATIN. | PRAVASTATIN | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 20 | C | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
127804031 | 12780403 | 21 | C | ASA | ASPIRIN | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127804031 | 12780403 | 1 | Hypertension |
127804031 | 12780403 | 2 | Gout |
127804031 | 12780403 | 3 | Osteoarthritis |
127804031 | 12780403 | 4 | Rheumatoid arthritis |
127804031 | 12780403 | 5 | Osteoarthritis |
127804031 | 12780403 | 6 | Rheumatoid arthritis |
127804031 | 12780403 | 7 | Osteoarthritis |
127804031 | 12780403 | 8 | Rheumatoid arthritis |
127804031 | 12780403 | 9 | Osteoarthritis |
127804031 | 12780403 | 10 | Product used for unknown indication |
127804031 | 12780403 | 11 | Product used for unknown indication |
127804031 | 12780403 | 12 | Product used for unknown indication |
127804031 | 12780403 | 13 | Product used for unknown indication |
127804031 | 12780403 | 14 | Product used for unknown indication |
127804031 | 12780403 | 15 | Product used for unknown indication |
127804031 | 12780403 | 16 | Product used for unknown indication |
127804031 | 12780403 | 17 | Product used for unknown indication |
127804031 | 12780403 | 18 | Product used for unknown indication |
127804031 | 12780403 | 19 | Product used for unknown indication |
127804031 | 12780403 | 20 | Product used for unknown indication |
127804031 | 12780403 | 21 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127804031 | 12780403 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127804031 | 12780403 | Acute kidney injury |
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 |
---|---|---|---|---|---|---|
127804031 | 12780403 | 1 | 201301 | 20130806 | 0 | |
127804031 | 12780403 | 2 | 201301 | 20130806 | 0 | |
127804031 | 12780403 | 3 | 201301 | 20130806 | 0 | |
127804031 | 12780403 | 4 | 20100901 | 20101006 | 0 | |
127804031 | 12780403 | 6 | 20100901 | 20101006 | 0 | |
127804031 | 12780403 | 8 | 20100901 | 20101006 | 0 |