FDA Alerts
FDA Alerts
06/13/2016
A study examined the consequences of an FDA warning recommending against the prescription of the antidepressant citalopram at dosages higher than 40 mg/day.
06/13/2016
FDA Alerts
FDA Alerts
06/13/2016
A study examined the consequences of an FDA warning recommending against the prescription of the antidepressant citalopram at dosages higher than 40 mg/day.
06/13/2016
FDA Alerts
FDA Alerts
06/13/2016
A study examined the consequences of an FDA warning recommending against the prescription of the antidepressant citalopram at dosages higher than 40 mg/day.
06/13/2016
Gastroenterology
Gastroenterology
06/08/2016
The FDA has issued a warning of serious and potentially fatal cardiac problems associated with the higher-than-recommended use of the antidiarrheal drug loperamide (Imodium).
06/08/2016
Gastroenterology
Gastroenterology
06/08/2016
The FDA has issued a warning of serious and potentially fatal cardiac problems associated with the higher-than-recommended use of the antidiarrheal drug loperamide (Imodium).
06/08/2016
Gastroenterology
Gastroenterology
06/08/2016
The FDA has issued a warning of serious and potentially fatal cardiac problems associated with the higher-than-recommended use of the antidiarrheal drug loperamide (Imodium).
06/08/2016
Prostate Cancer
Prostate Cancer
05/31/2016
Primary care practitioners should be aware of 3 new FDA approvals that may be useful when treating patients with opioid dependence, prostate cancer, and multiple sclerosis.
05/31/2016
FDA Alerts
FDA Alerts
05/13/2016
A safety review showed that when fluoroquinolones were used systemically, they were associated with disabling and potentially permanent serious adverse effects.
05/13/2016
FDA Alerts
FDA Alerts
05/13/2016
A safety review showed that when fluoroquinolones were used systemically, they were associated with disabling and potentially permanent serious adverse effects.
05/13/2016
FDA Alerts
FDA Alerts
05/13/2016
A safety review showed that when fluoroquinolones were used systemically, they were associated with disabling and potentially permanent serious adverse effects.
05/13/2016