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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
99238401 | 9923840 | 1 | I | 20140116 | 20140225 | 20140225 | PER | US-AMGEN-USASP2014003733 | AMGEN | 38.00 | YR | F | Y | 72.00000 | KG | 20140225 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
99238401 | 9923840 | 1 | PS | Enbrel | 1 | SUBCUTANEOUS | 50 MG, QWK | D | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | ||||||
99238401 | 9923840 | 2 | C | METHOTREXATE | 1 | 2.5 MG, UNK | D | 0 | 2.5 | MG | TABLET | ||||||||
99238401 | 9923840 | 3 | C | SYNTHROID | 1 | 50 MUG, UNK | D | 0 | 50 | UG | TABLET | ||||||||
99238401 | 9923840 | 4 | C | BIOTIN | 1 | 2500 MUG, UNK | D | 0 | 2500 | UG | CAPSULE | ||||||||
99238401 | 9923840 | 5 | C | FOLIC ACID | 1 | UNK | D | 0 | TABLET | ||||||||||
99238401 | 9923840 | 6 | C | VITAMIN B | 1 | UNK | D | 0 | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
99238401 | 9923840 | 1 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
99238401 | 9923840 | Cough | |
99238401 | 9923840 | Ear pain | |
99238401 | 9923840 | Nasal congestion | |
99238401 | 9923840 | Pyrexia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |