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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127506291 | 12750629 | 1 | I | 20160909 | 20160916 | 20160916 | EXP | BR-PFIZER INC-2016429274 | PFIZER | 85.00 | YR | M | Y | 65.00000 | KG | 20160916 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127506291 | 12750629 | 1 | PS | XALATAN | LATANOPROST | 1 | Ophthalmic | 1 DROP IN EACH EYE (3UG), UNSPECIFIED FREQUENCY | U | 20597 | 3 | UG | EYE DROPS, SOLUTION | ||||||
| 127506291 | 12750629 | 2 | C | TIMOLOL MALEATE. | TIMOLOL MALEATE | 1 | Ophthalmic | 1 DROP IN EACH EVERY 12 HOURS | 0 | 2 | GTT | BID | |||||||
| 127506291 | 12750629 | 3 | C | NEOVITE LUTEIN | 2 | Oral | 2 DRAGGES PER DAY | 0 | 2 | DF | |||||||||
| 127506291 | 12750629 | 4 | C | LOSARTAN. | LOSARTAN | 1 | Oral | 2 TABLETS, DAILY | 0 | 2 | DF | ||||||||
| 127506291 | 12750629 | 5 | C | LOSARTAN. | LOSARTAN | 1 | 1 UNK, UNK | 0 | 1 | DF | |||||||||
| 127506291 | 12750629 | 6 | C | SOMALGIN | ASPIRINDIHYDROXYALUMINUM AMINOACETATE ANHYDROUSMAGNESIUM CARBONATE | 1 | Oral | UNK UNK, 1X/DAY | 0 | QD | |||||||||
| 127506291 | 12750629 | 7 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | UNK, 1X/DAY | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127506291 | 12750629 | 3 | Visual impairment |
| 127506291 | 12750629 | 4 | Hypertension |
| 127506291 | 12750629 | 6 | Anticoagulant therapy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127506291 | 12750629 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127506291 | 12750629 | Drug dose omission | |
| 127506291 | 12750629 | Vision blurred | |
| 127506291 | 12750629 | Visual acuity reduced |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127506291 | 12750629 | 1 | 2013 | 0 | ||
| 127506291 | 12750629 | 2 | 201601 | 0 | ||
| 127506291 | 12750629 | 3 | 2011 | 0 | ||
| 127506291 | 12750629 | 4 | 2006 | 0 | ||
| 127506291 | 12750629 | 6 | 2006 | 0 | ||
| 127506291 | 12750629 | 7 | 2014 | 0 |