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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127709601 | 12770960 | 1 | I | 20160915 | 20160922 | 20160922 | EXP | US-PFIZER INC-2016437919 | PFIZER | 72.00 | YR | F | Y | 77.00000 | KG | 20160922 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127709601 | 12770960 | 1 | PS | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | UNK | U | 20699 | PROLONGED-RELEASE CAPSULE | ||||||||
127709601 | 12770960 | 2 | SS | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | U | 20699 | PROLONGED-RELEASE CAPSULE | ||||||||||
127709601 | 12770960 | 3 | SS | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | U | 20699 | PROLONGED-RELEASE CAPSULE | ||||||||||
127709601 | 12770960 | 4 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Oral | 0.75 MG, 1X/DAY | 0 | .75 | MG | TABLET | QD | ||||||
127709601 | 12770960 | 5 | C | FETZIMA | LEVOMILNACIPRAN HYDROCHLORIDE | 1 | Oral | 80 MG, 1X/DAY | 0 | 80 | MG | CAPSULE | QD | ||||||
127709601 | 12770960 | 6 | C | FETZIMA | LEVOMILNACIPRAN HYDROCHLORIDE | 1 | Oral | 40 MG, UNK | 0 | 40 | MG | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127709601 | 12770960 | 1 | Depression |
127709601 | 12770960 | 2 | Anxiety |
127709601 | 12770960 | 3 | Post-traumatic stress disorder |
127709601 | 12770960 | 4 | Thyroid disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127709601 | 12770960 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127709601 | 12770960 | Cerebral disorder | |
127709601 | 12770960 | Depression | |
127709601 | 12770960 | Drug dependence | |
127709601 | 12770960 | Feeling abnormal | |
127709601 | 12770960 | Headache | |
127709601 | 12770960 | Hyperhidrosis | |
127709601 | 12770960 | Intentional product misuse |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |