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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121435721 | 12143572 | 1 | I | 20160209 | 20160304 | 20160304 | PER | US-JNJFOC-20160209756 | JANSSEN | 86.00 | YR | E | F | Y | 54.43000 | KG | 20160304 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121435721 | 12143572 | 1 | PS | WOMENS ROGAINE UNSCENTED | MINOXIDIL | 1 | Topical | N | 0174D3A | 999999 | FOAM | ||||||||
121435721 | 12143572 | 2 | SS | WOMENS ROGAINE UNSCENTED | MINOXIDIL | 1 | Topical | N | 0174D3A | 21812 | FOAM |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121435721 | 12143572 | 2 | Alopecia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121435721 | 12143572 | Incorrect dose administered | |
121435721 | 12143572 | Product quality issue | |
121435721 | 12143572 | Product use issue | |
121435721 | 12143572 | Skin discolouration | |
121435721 | 12143572 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |