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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4329079 | 4121191 | I | 4329079-2 | 20040303 | 20040331 | DIR | M | N | 195 | LBS | 20040330 | N | Y |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4329079 | 1004752514 | PS | FUZEON | 1 | N | Y |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4329079 | 1004752514 | ACQUIRED IMMUNODEFICIENCY SYNDROME |
Outcome of event
Event ID | OUTC COD |
---|---|
4329079 | DS |
Reactions reported
Event ID | PT |
---|---|
4329079 | CONTUSION |
4329079 | CSF TEST ABNORMAL |
4329079 | DIFFICULTY IN WALKING |
4329079 | HYPERAESTHESIA |
4329079 | INJECTION SITE ERYTHEMA |
4329079 | INJECTION SITE HAEMORRHAGE |
4329079 | INSOMNIA |
4329079 | MUSCLE STRAIN |
4329079 | MYALGIA |
4329079 | PAIN |
4329079 | SKIN BLEEDING |
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 |
---|---|---|---|---|---|
4329079 | 1004752514 | 20010206 | 20040330 |