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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8248786 | 8483711 | F | 8248786-2 | 20110901 | 20120321 | 20120331 | EXP | US-ALLERGAN-1203596US | ALLERGANFDA | 39 | YR | F | Y | 20120331 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8248786 | 1019282888 | SS | LATISSE | 1 | 70542 | 022369 | |||||
8248786 | 1019282889 | C | VISINE /00256502/ | 2 | OPHTHALMIC | 2 GTT, PRN | |||||
8248786 | 1019282887 | PS | LATISSE | 1 | TOPICAL | 2 GTT, QHS FOR ONE AND ONE HALF YEARS | 70542 | 022369 | |||
8248786 | 1019282890 | C | VISINE /00256502/ | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8248786 | 1019282889 | DRY EYE |
8248786 | 1019282887 | GROWTH OF EYELASHES |
8248786 | 1019282890 | ERYTHEMA |
Outcome of event
Event ID | OUTC COD |
---|---|
8248786 | OT |
Reactions reported
Event ID | PT |
---|---|
8248786 | FAECES DISCOLOURED |
8248786 | NAUSEA |
8248786 | HEADACHE |
8248786 | STILLBIRTH |
8248786 | TRICHORRHEXIS |
8248786 | OCULAR HYPERAEMIA |
8248786 | DECREASED APPETITE |
8248786 | MUCOUS STOOLS |
8248786 | WRONG TECHNIQUE IN DRUG USAGE PROCESS |
8248786 | MATERNAL EXPOSURE DURING PREGNANCY |
8248786 | PRURITUS |
8248786 | DIARRHOEA HAEMORRHAGIC |
8248786 | EYE PRURITUS |
8248786 | ERYTHEMA |
8248786 | EYE PAIN |
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 |
---|---|---|---|---|---|
8248786 | 1019282889 | 20110401 | |||
8248786 | 1019282887 | 20100101 | 20111001 |