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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6390604 | 7141189 | F | 6390604-1 | 20090901 | 20090925 | 20091006 | EXP | US-JNJFOC-20090908821 | MCNEIL CONSUMER HEALTHCARE | 3 | YR | M | Y | 14.97 | KG | 20091006 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6390604 | 1012385435 | PS | CHILDREN'S TYLENOL SUSPENSION | 1 | ORAL | SCM029 | 19872 | ||||
6390604 | 1012385436 | SS | CHILDREN'S TYLENOL SUSPENSION | 1 | ORAL | SCM029 | 19872 | ||||
6390604 | 1012385437 | C | CHILDREN'S MOTRIN | 1 | 19872 | ||||||
6390604 | 1012385438 | C | AUGMENTIN '125' | 1 | 19872 | ||||||
6390604 | 1012385439 | C | QVAR INHALER | 2 | 19872 | ||||||
6390604 | 1012385440 | C | ALBUTEROL | 1 | 19872 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6390604 | 1012385436 | PYREXIA |
6390604 | 1012385437 | PYREXIA |
6390604 | 1012385438 | BACTERIAL INFECTION |
6390604 | 1012385439 | ASTHMA |
6390604 | 1012385440 | ASTHMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6390604 | OT |
Reactions reported
Event ID | PT |
---|---|
6390604 | DRUG INEFFECTIVE |
6390604 | PRODUCT QUALITY ISSUE |
6390604 | TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |