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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121713115 | 12171311 | 5 | F | 2016 | 20160906 | 20160311 | 20160913 | PER | US-PFIZER INC-2016108785 | PFIZER | 79.00 | YR | F | Y | 73.00000 | KG | 20160913 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121713115 | 12171311 | 1 | PS | PREMPRO | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | Oral | 1 DF (1.25 MG/2.5 MG), 1X/DAY | 20527 | 1 | DF | TABLET | QD | ||||||
| 121713115 | 12171311 | 2 | SS | PREMPRO | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | 1 DF, 1X/DAY | 20527 | 1 | DF | TABLET | QD | |||||||
| 121713115 | 12171311 | 3 | C | VITAMIN C | ASCORBIC ACID | 1 | UNK | 0 | |||||||||||
| 121713115 | 12171311 | 4 | C | VITAMIN B | VITAMIN B | 1 | UNK | 0 | |||||||||||
| 121713115 | 12171311 | 5 | C | CALCIUM | CALCIUM | 1 | UNK | 0 | |||||||||||
| 121713115 | 12171311 | 6 | C | MAGNESIUM | MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 121713115 | 12171311 | 7 | C | GLUCOSAMINE | GLUCOSAMINE | 1 | 1 DF, 1X/DAY | 0 | 1 | DF | QD | ||||||||
| 121713115 | 12171311 | 8 | C | VITAMIN E | .ALPHA.-TOCOPHEROL | 1 | 1 DF, 2X/WEEK | 0 | 1 | DF | BIW |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121713115 | 12171311 | 1 | Perinatal depression |
| 121713115 | 12171311 | 2 | Depression |
| 121713115 | 12171311 | 7 | Bone disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121713115 | 12171311 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121713115 | 12171311 | Arthralgia | |
| 121713115 | 12171311 | Bone pain | |
| 121713115 | 12171311 | Depression | |
| 121713115 | 12171311 | Fatigue | |
| 121713115 | 12171311 | Hyperhidrosis | |
| 121713115 | 12171311 | Incorrect dose administered | |
| 121713115 | 12171311 | Menopausal symptoms | |
| 121713115 | 12171311 | Night sweats | |
| 121713115 | 12171311 | Postmenopausal haemorrhage | |
| 121713115 | 12171311 | Product use issue | |
| 121713115 | 12171311 | Seasonal affective disorder | |
| 121713115 | 12171311 | Sleep disorder |
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 |
|---|---|---|---|---|---|---|
| 121713115 | 12171311 | 1 | 20160212 | 0 | ||
| 121713115 | 12171311 | 2 | 201606 | 0 |