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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6086216 | 6921607 | I | 6086216-X | 20090202 | 20090218 | DIR | 17 | YR | F | N | 117 | LBS | 20090217 | CN | N | Y | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6086216 | 1011159555 | PS | OCELLA 3MG/0.03MG BARR | 2 | ORAL | ONE DAILY PO | D | 82329A | 20110201 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6086216 | 1011159555 | PREMENSTRUAL SYNDROME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6086216 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6086216 | ABNORMAL BEHAVIOUR |
| 6086216 | ACTIVITIES OF DAILY LIVING IMPAIRED |
| 6086216 | ANOREXIA |
| 6086216 | ARRHYTHMIA |
| 6086216 | ASTHENIA |
| 6086216 | BREAST PAIN |
| 6086216 | BREAST SWELLING |
| 6086216 | DISTURBANCE IN ATTENTION |
| 6086216 | DIZZINESS |
| 6086216 | EDUCATIONAL PROBLEM |
| 6086216 | HEADACHE |
| 6086216 | MALAISE |
| 6086216 | MUSCLE SPASMS |
| 6086216 | NAUSEA |
| 6086216 | OROPHARYNGEAL PAIN |
| 6086216 | PALLOR |
| 6086216 | PRURITUS |
| 6086216 | PYREXIA |
| 6086216 | SWELLING FACE |
| 6086216 | URINARY TRACT INFECTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6086216 | 1011159555 | 20090202 |