Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5229712 | 6231104 | I | 5229712-7 | 20070124 | 20070206 | EXP | JP-PFIZER INC-2007007902 | PFIZER INC | Y | 20070206 | PH | JAPAN |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5229712 | 1008117664 | PS | ZITHROMAC | 2 | ORAL | 50710 | |||||
5229712 | 1008117665 | C | HOKUNALIN | 2 | ORAL | ||||||
5229712 | 1008117666 | C | MUCODYNE | 2 | ORAL | ||||||
5229712 | 1008117667 | C | PERIACTIN | 1 | ORAL | ||||||
5229712 | 1008117668 | C | ASVERIN | 2 | ORAL |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5229712 | OT |
Reactions reported
Event ID | PT |
---|---|
5229712 | EPISTAXIS |
5229712 | EYE HAEMORRHAGE |
5229712 | OCULAR HYPERAEMIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |