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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6386384 | 7144002 | I | 6386384-6 | 20090923 | 20090930 | DIR | F | N | 3.445 | KG | 20090929 | PH | Y | N | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6386384 | 1012369962 | PS | GENTAK | 1 | OPHTHALMIC | 1 APPLICATION ONCE OPHTHALMIC | D | D | 9F13A | 20110531 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6386384 | 1012369962 | OPHTHALMIA NEONATORUM |
6386384 | 1012369962 | PROPHYLAXIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6386384 | EYELID DISORDER |
6386384 | SKIN REACTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6386384 | 1012369962 | 20090923 | 20090923 |