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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112533072 | 11253307 | 2 | F | 20150623 | 20150709 | 20160711 | PER | US-TEVA-565912USA | TEVA | 0.00 | F | Y | 0.00000 | 20160711 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112533072 | 11253307 | 1 | PS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 150 MILLIGRAM DAILY; | Y | 76565 | 150 | MG | CAPSULE | QD | |||||
112533072 | 11253307 | 2 | SS | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 150 MILLIGRAM DAILY; | 0 | 150 | MG | CAPSULE | QD | ||||||
112533072 | 11253307 | 3 | C | LISINOPRIL. | LISINOPRIL | 1 | Oral | 20 MILLIGRAM DAILY; | 0 | 20 | MG | TABLET | QD | ||||||
112533072 | 11253307 | 4 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Oral | 5 MILLIGRAM DAILY; | 0 | 5 | MG | TABLET | QD | ||||||
112533072 | 11253307 | 5 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Oral | 500 MILLIGRAM DAILY; | 0 | 500 | MG | TABLET | QD | ||||||
112533072 | 11253307 | 6 | C | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | ONCE A DAY AS NEEDED | 0 | 30 | MG | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
112533072 | 11253307 | 1 | Anxiety |
112533072 | 11253307 | 2 | Anxiety |
112533072 | 11253307 | 3 | Hypertension |
112533072 | 11253307 | 4 | Fluid overload |
112533072 | 11253307 | 5 | Glucose tolerance impaired |
112533072 | 11253307 | 6 | Attention deficit/hyperactivity disorder |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
112533072 | 11253307 | Drug effect decreased | |
112533072 | 11253307 | Feeling abnormal | |
112533072 | 11253307 | Feeling of despair | |
112533072 | 11253307 | Hypertension | |
112533072 | 11253307 | Intentional product misuse | |
112533072 | 11253307 | Mood altered | |
112533072 | 11253307 | Product substitution issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |