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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125387911 | 12538791 | 1 | I | 20160624 | 20160708 | 20160708 | EXP | DE-AUROBINDO-AUR-APL-2016-08504 | AUROBINDO | 0.00 | Y | 0.00000 | 20160708 | CN | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125387911 | 12538791 | 1 | PS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Unknown | 150 MG, UNK | U | U | 90555 | 150 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125387911 | 12538791 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125387911 | 12538791 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125387911 | 12538791 | Crying | |
| 125387911 | 12538791 | Dizziness | |
| 125387911 | 12538791 | Emotional disorder | |
| 125387911 | 12538791 | Feeling of body temperature change | |
| 125387911 | 12538791 | Headache | |
| 125387911 | 12538791 | Hyperhidrosis | |
| 125387911 | 12538791 | Irritability | |
| 125387911 | 12538791 | Limb discomfort | |
| 125387911 | 12538791 | Nasopharyngitis | |
| 125387911 | 12538791 | Rebound effect | |
| 125387911 | 12538791 | Tinnitus |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |