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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125367373 | 12536737 | 3 | F | 200104 | 20160727 | 20160707 | 20160802 | EXP | GB-BAUSCH-BL-2016-015593 | BAUSCH AND LOMB | 41.00 | YR | F | Y | 0.00000 | 20160802 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125367373 | 12536737 | 1 | PS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | U | 40070 | ||||||||||
| 125367373 | 12536737 | 2 | SS | PAROXETINE. | PAROXETINE | 1 | Unknown | U | 0 | 30 | MG | QD | |||||||
| 125367373 | 12536737 | 3 | SS | PAROXETINE. | PAROXETINE | 1 | Unknown | U | 0 | 20 | MG | TABLET | QD | ||||||
| 125367373 | 12536737 | 4 | SS | PAROXETINE. | PAROXETINE | 1 | Unknown | U | 0 | 30 | MG | QD | |||||||
| 125367373 | 12536737 | 5 | SS | TRANYLCYPROMINE | TRANYLCYPROMINE | 1 | Unknown | U | 0 | ||||||||||
| 125367373 | 12536737 | 6 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Endocervical | U | 0 | 20 | MG | ||||||||
| 125367373 | 12536737 | 7 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Unknown | U | 0 | 30 | MG | ||||||||
| 125367373 | 12536737 | 8 | C | PROCHLORPERAZINE. | PROCHLORPERAZINE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125367373 | 12536737 | 1 | Asthma |
| 125367373 | 12536737 | 2 | Depression |
| 125367373 | 12536737 | 5 | Product used for unknown indication |
| 125367373 | 12536737 | 6 | Depression |
| 125367373 | 12536737 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125367373 | 12536737 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125367373 | 12536737 | Anger | |
| 125367373 | 12536737 | Anxiety | |
| 125367373 | 12536737 | Condition aggravated | |
| 125367373 | 12536737 | Dizziness | |
| 125367373 | 12536737 | Drug withdrawal syndrome | |
| 125367373 | 12536737 | Dyssomnia | |
| 125367373 | 12536737 | Feeling cold | |
| 125367373 | 12536737 | Headache | |
| 125367373 | 12536737 | Hot flush | |
| 125367373 | 12536737 | Hyperhidrosis | |
| 125367373 | 12536737 | Hypoaesthesia | |
| 125367373 | 12536737 | Mood swings | |
| 125367373 | 12536737 | Muscle spasms | |
| 125367373 | 12536737 | Nausea | |
| 125367373 | 12536737 | Obsessive-compulsive disorder | |
| 125367373 | 12536737 | Paraesthesia | |
| 125367373 | 12536737 | Suicidal ideation | |
| 125367373 | 12536737 | Vomiting | |
| 125367373 | 12536737 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 125367373 | 12536737 | 2 | 20010126 | 20010608 | 0 | |
| 125367373 | 12536737 | 3 | 20001127 | 20010608 | 0 | |
| 125367373 | 12536737 | 4 | 200011 | 2001 | 0 | |
| 125367373 | 12536737 | 6 | 20001127 | 20010608 | 0 |