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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127219661 | 12721966 | 1 | I | 20160831 | 20160907 | 20160907 | PER | US-PFIZER INC-2016415220 | PFIZER | 0.00 | F | Y | 0.00000 | 20160907 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127219661 | 12721966 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 100 MG, DAILY | N | 21992 | 100 | MG | PROLONGED-RELEASE TABLET | ||||||
| 127219661 | 12721966 | 2 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 50 MG, 1X/DAY | N | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | QD | |||||
| 127219661 | 12721966 | 3 | C | UNITHROID | LEVOTHYROXINE SODIUM | 1 | Oral | 125 MG, 1X/DAY | 0 | 125 | MG | TABLET | QD | ||||||
| 127219661 | 12721966 | 4 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 1.25 MG, WEEKLY | 0 | 1.25 | MG | CAPSULE | /wk | ||||||
| 127219661 | 12721966 | 5 | C | PROLIA | DENOSUMAB | 1 | SHOT TWICE A YEAR | 0 | INJECTION | ||||||||||
| 127219661 | 12721966 | 6 | C | PROLIA | DENOSUMAB | 1 | 0 | INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127219661 | 12721966 | 1 | Depression |
| 127219661 | 12721966 | 3 | Thyroid disorder |
| 127219661 | 12721966 | 4 | Osteoporosis |
| 127219661 | 12721966 | 5 | Osteoporosis |
| 127219661 | 12721966 | 6 | Bone density abnormal |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127219661 | 12721966 | Abnormal dreams | |
| 127219661 | 12721966 | Anxiety | |
| 127219661 | 12721966 | Diarrhoea | |
| 127219661 | 12721966 | Dizziness | |
| 127219661 | 12721966 | Fatigue | |
| 127219661 | 12721966 | Hot flush | |
| 127219661 | 12721966 | Hyperhidrosis | |
| 127219661 | 12721966 | Somnolence | |
| 127219661 | 12721966 | Tinnitus |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |