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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117883782 | 11788378 | 2 | F | 2008 | 20151007 | 20151201 | 20160823 | PER | US-TEVA-599439USA | TEVA | 0.00 | F | Y | 98.00000 | KG | 20160823 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117883782 | 11788378 | 1 | PS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Unknown | Y | 76690 | 37.5 | MG | ||||||||
| 117883782 | 11788378 | 2 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 117883782 | 11788378 | 3 | SS | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Unknown | 30 MILLIGRAM DAILY; | 0 | 30 | MG | QD | |||||||
| 117883782 | 11788378 | 4 | C | ATENOLOL. | ATENOLOL | 1 | Oral | 25 MILLIGRAM DAILY; | 0 | 25 | MG | QD | |||||||
| 117883782 | 11788378 | 5 | C | LISINOPRIL AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDELISINOPRIL | 1 | 10/12.5 | 0 | BID | ||||||||||
| 117883782 | 11788378 | 6 | C | PROMETHAZINE | PROMETHAZINEPROMETHAZINE HYDROCHLORIDE | 1 | 50 MILLIGRAM DAILY; | 0 | 25 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117883782 | 11788378 | 1 | Death of relative |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117883782 | 11788378 | Asthenia | |
| 117883782 | 11788378 | Asthma | |
| 117883782 | 11788378 | Blood cholesterol increased | |
| 117883782 | 11788378 | Blood pressure increased | |
| 117883782 | 11788378 | Diarrhoea | |
| 117883782 | 11788378 | Drug ineffective | |
| 117883782 | 11788378 | Feeling jittery | |
| 117883782 | 11788378 | Hyperhidrosis | |
| 117883782 | 11788378 | Inappropriate schedule of drug administration | |
| 117883782 | 11788378 | Insomnia | |
| 117883782 | 11788378 | Malaise | |
| 117883782 | 11788378 | Muscle spasms | |
| 117883782 | 11788378 | Musculoskeletal stiffness | |
| 117883782 | 11788378 | Nausea | |
| 117883782 | 11788378 | Nervousness | |
| 117883782 | 11788378 | Paraesthesia | |
| 117883782 | 11788378 | Sleep apnoea syndrome | |
| 117883782 | 11788378 | Vomiting | |
| 117883782 | 11788378 | 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 |
|---|---|---|---|---|---|---|
| 117883782 | 11788378 | 1 | 2008 | 0 |