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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126560101 | 12656010 | 1 | I | 20160520 | 20160816 | 20160816 | PER | US-ROCHE-1761918 | ROCHE | 0.00 | F | Y | 0.00000 | 20160816 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126560101 | 12656010 | 1 | PS | PEGASYS | PEGINTERFERON ALFA-2A | 1 | Subcutaneous | B3025B10 | 103964 | 180 | MG | /wk | |||||||
126560101 | 12656010 | 2 | C | CEPHALEXIN. | CEPHALEXIN | 1 | Unknown | 0 | 500 | MG | CAPSULE | ||||||||
126560101 | 12656010 | 3 | C | LABETALOL | LABETALOLLABETALOL HYDROCHLORIDE | 1 | Unknown | 0 | 100 | MG | TABLET | ||||||||
126560101 | 12656010 | 4 | C | PHENTERMINE. | PHENTERMINE | 1 | Unknown | 0 | 37.5 | MG | TABLET | ||||||||
126560101 | 12656010 | 5 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | 0 | 600 | MG | TABLET | ||||||||
126560101 | 12656010 | 6 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | 0 | 10 | MG | TABLET | ||||||||
126560101 | 12656010 | 7 | C | METRONIDAZOL | METRONIDAZOLE | 1 | Unknown | 0 | 500 | MG | TABLET | ||||||||
126560101 | 12656010 | 8 | C | ENOXAPARIN | ENOXAPARIN | 1 | Unknown | 40/0.4 ML | 0 | ||||||||||
126560101 | 12656010 | 9 | C | PROGESTERONE. | PROGESTERONE | 1 | Unknown | 0 | 200 | MG | CAPSULE | ||||||||
126560101 | 12656010 | 10 | C | LOVENOX | ENOXAPARIN SODIUM | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126560101 | 12656010 | 1 | Thrombolysis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126560101 | 12656010 | No adverse event | |
126560101 | 12656010 | Pregnancy |
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 |
---|---|---|---|---|---|---|
126560101 | 12656010 | 1 | 20160311 | 201604 | 0 |