Personal Injury Lawyers
Toll Free 24/7
877-DRUG-GIANT
(877) 378-4442 816-LAW-FIRM
(816) 529-3476

Pharmaceutical Litigation

Medical Devices

Personal Injury

Nursing Home Litigation

Pollutants & Toxic Chemical Exposure

Defective & Recalled Products

Medical Malpractice

CONSUMER PROTECTION

Areas of Practice

Pharmaceutical Litigation

Accolate®

Manufacturer: AstraZeneca Pharmaceuticals
Uses: A non-steroidal tablet for the prevention and continuous treatment of asthma in adults


More Information

Accolate
Accolate

Accolate manufacturer AstraZeneca warned that Accolate side effects were potentially deadly. Accolate side effects included severe liver damage. First surfacing in the beginning of 2000, Accolate side effects had been more closely monitored by the FDA. The FDA told AstraZeneca to alert physicians of the dangerous Accolate side effects in September 2000. The company did not send out official FDA warnings regarding Accolate side effects, but instead just sent out physician notices in that month's Physician's Desk Reference.


Side Effects

Hepatotoxicity- Cases of life-threatening hepatic failure have been reported in patients treated with Accolate. Patients should be advised to be alert for signs and symptoms of liver dysfunction (e.g., right upper quadrant abdominal pain, nausea, fatigue, lethargy, pruritus, jaundice, flu-like symptoms, and anorexia) and to contact their physician immediately if they occur.

For more information:
Pharmaceutical Litigation
Prescription Injury FAQs
Pharmaceutical Legal Glossary


Click Here For A Free Case Evaluation

Watch Our Video
You need to upgrade your Flash Player Click here to download the latest version of the Flash Player.
Click to Call to Speak with Our Injury Lawyers Today
FREE CASE REVIEW

We understand that you have questions and need answers. Our attorneys and staff are available to help you find the information you need.

Name:
Phone:
Email:
How did you hear about us?
Comment / Questions:

graphic
No Recovery No Fees
Recall News
MEDTRONIC LEAD RECALL!

The FDA released a statement on Medtronic's decision to suspend distribution of its Sprint Fidelis defibrillation leads due to a number of fractures which have been detected. These devices have a reasonable probability that if a particular device is malfunctioning, the device will cause serious bodily injury or death.

Product Recall
NEWS HEADLINES
Recent Headlines
NEWS HEADLINES

The Peterson Foundation, Inc. was established by David M. Peterson to support children in need throughout the Kansas City area. For more information click here.

News