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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5040493 | 6034755 | F | 5040493-2 | 20060320 | 20060630 | EXP | US-ROCHE-441347 | ROCHE | 42 | YR | M | Y | 20060630 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5040493 | 1007431397 | PS | PEGASYS | 1 | UNKNOWN | STARTED WITH A DOSE HIGHER THAN 90 MCG. | |||||
5040493 | 1007431398 | SS | PEGASYS | 1 | UNKNOWN | REDUCED DOSE. | |||||
5040493 | 1007431399 | SS | PEGASYS | 1 | UNKNOWN | ||||||
5040493 | 1007431400 | SS | COPEGUS | 1 | ORAL | 021511 | |||||
5040493 | 1007431401 | C | ELAVIL | 1 | |||||||
5040493 | 1007431402 | C | KEFLEX | 1 | |||||||
5040493 | 1007431403 | C | CIPRO | 1 | |||||||
5040493 | 1007431404 | C | LOPRESSOR | 1 | ORAL | ||||||
5040493 | 1007431405 | C | NORVASC | 1 | ORAL | ||||||
5040493 | 1007431406 | C | 1 MEDICINE | 2 | DRUG NAME: 'HYPERTHYROID MEDICINE' |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5040493 | 1007431401 | INSOMNIA |
5040493 | 1007431402 | LUNG INFECTION |
5040493 | 1007431403 | LUNG INFECTION |
5040493 | 1007431404 | HYPERTENSION |
5040493 | 1007431405 | HYPERTENSION |
5040493 | 1007431406 | HYPERTHYROIDISM |
Outcome of event
Event ID | OUTC COD |
---|---|
5040493 | OT |
Reactions reported
Event ID | PT |
---|---|
5040493 | BLOOD PRESSURE DIASTOLIC INCREASED |
5040493 | BLOOD THYROID STIMULATING HORMONE INCREASED |
5040493 | CARPAL TUNNEL SYNDROME |
5040493 | LUNG INFECTION |
5040493 | THYROIDECTOMY |
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 |
---|---|---|---|---|---|
5040493 | 1007431398 | 20051202 | |||
5040493 | 1007431400 | 20051202 |