Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6919192 | 7536925 | I | 6919192-5 | 20100802 | 20100811 | EXP | BR-PFIZER INC-2010098424 | PFIZERINC | YR | F | Y | 63 | KG | 20100811 | CN | BRAZIL |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6919192 | 1014393344 | PS | DEPO-PROVERA | 1 | INTRAMUSCULAR | 150 MG, EVERY 3 MONTHS | 020246 | ||||
| 6919192 | 1014393345 | SS | DEPO-PROVERA | 1 | 020246 | ||||||
| 6919192 | 1014393346 | SS | DEPO-PROVERA | 1 | 020246 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6919192 | 1014393344 | CONTRACEPTION |
| 6919192 | 1014393345 | OFF LABEL USE |
| 6919192 | 1014393346 | MENSTRUAL DISCOMFORT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6919192 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6919192 | AMENORRHOEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |