What We Do
Defective Medical Products
- Medicines
- Accutane Lawsuit
- AMO Complete Moistureplus Recall
- Apothecure Colchicine Lawsuit
- Baxter Heparin Recall and Lawsuit
- Bismacine Chromacine
- Botox
- Carbinoxamine
- Chromium Poisoning (Toxicity)
- Colchicine Recall Lawyer
- Colistimethate Lawsuit Lawyer
- Edetate Disodium
- Fentanyl
- Fentanyl Patch Recall
- Fentora
- Fleet Lawsuit - Phosphate Nephropathy
- Fosamax Osteonecrosis Jaw
- Ketek Liver Failure
- Ortho Evra Birth Control Patch
- Promethazine
- Rocephin Death
- Selenium Poisoning (Toxicity)
- Topical Anesthetic
- Total Body Formula Recall and Lawsuit
- Trasylol and Kidney Failure
- Trasylol - Lawyer and Lawsuit
- Trasylol Recall
- Tysabri Lawsuit - No Recall
- Zelnorm Heart Attack Stroke Lawsuit
- Medical Equipment
- Medtronic Defibrillator Leads
- Medtronic Lawsuit
- Medtronic Lawyer
- Guidant Recalls
- Free Guidant Recall Consultation
- Guidant Ancure
- Guidant Lawsuit Recall
- Guidant Pacemaker Defibrillator Defect
- Guidant Pacemaker Recall
- FDA Pacemaker Defibrillator Statement
- Infusion Pump
- FDA Recalls
- News & Topics
- Archives
Welcome to Pritzker | Ruohonen
Fentora
FENTORA LAWSUIT INFORMATION: There have been serious, adverse events, including deaths, in patients treated with FENTORA (fentanyl buccal tablet). The active ingredient in FENTORA is fentanyl, an opiate used for pain that is about 80 times more potent than morphine. Fentanyl can be taken orally (FENTORA, Actiq, and other brands), administered intravenously, or slowly absorbed into the body through a skin patch (Duragesic and generics). In every form, fentanyl, the active ingredient in FENTORA, is inherently dangerous and extreme caution must be used by medical professionals.
Given the deaths associated with FENTORA, it appears some doctors and hospitals are not using reasonable care when prescribing and treating with FENTORA. According to the manufacturer of FENTORA, Cephalon, Inc., “These deaths occurred as a result of improper patient selection (e.g., use in opioid non-tolerant patients), improper dosing, and/or improper product substitution.”
If your family member died after taking FENTORA, you may have a claim against Cephalon and/or a medical malpractice claim against a doctor or hospital. If you retain Pritzker | Ruohonen to represent you, we will examine your medical records, consult with medical experts, and thoroughly investigate the death of your loved one. If our investigation provides adequate evidence, we will seek compensation from those responsible for your loved one’s death. We work on a contingency-fee basis, meaning you do not pay us unless we obtain a recovery for you.
To contact an attorney at Pritzker | Ruohonen regarding a FENTOR lawsuit, please call toll-free at 1-888-377-8900 or submit the firm’s online consultation form.
FENTORA and Medical Malpractice (Medication Error)
The following is key safety information provided by Cephalon regarding FENTORA. If your loved one’s doctor or hospital prescribed or administered FENTORA in a manner that did not meet these safety standards, you may have a medical malpractice claim (medication error) against the doctor or hospital. (A FENTORA overdose can lead to the death of the patient. If your loved one died, you may have a wrongful death claim.) The key safety information is as follows:
- Do prescribe FENTORA to patients who are opioid non-tolerant (i.e., patients who are not taking around-the-clock opioids). Was your loved one opioid non-tolerant? FENTORA is indicated only for the management of breakthrough pain in patients with cancer who are already receiving and who are tolerant to opioid therapy for their underlying persistent cancer pain. Patients considered opioid tolerant are those who are taking at least 60 mg oral morphine per day, at least 25 mcg transdermal fentany per hour, at least 30 mg of oral oxycodone daily, at least 8 mg oral hydromorphone daily or an equianalgesic dose of another opioid for a week or longer. If you retain Pritzker | Ruohonen, we will investigate this.
- Use FENTORA only for labeled indications
- Do not prescribe FENTORA for patients with acute pain, postoperative pain, headachelmigraine, or sports injuries, even if they are suitable for receiving other opioids on an as needed basis
- FENTORA is not a generic version of Actiq. Therefore, do NOT substitute FENTORA for Actiq or other fentanyl-containing products
- Follow dosage instructions, and educate your patients as to the importance of following these instructions carefully.
- For unrelieved breakthrough pain (BTP), patients should NOT take more than 2 FENTORA tablets per BTP episode
- Patients MUST wait at least 4 hours before treating another BTP episode with FENTORA
- For unrelieved breakthrough pain (BTP), patients should NOT take more than 2 FENTORA tablets per BTP episode
If you have questions regarding a FENTORA lawsuit, a lawyer at Pritzker | Ruohonen is available for a free consultation. To contact the firm, call toll-free at 1-888-377-8900 or submit the firm’s online consultation form.
Free Case Consultation
Firm News
Fred Pritzker Listed in The Best Lawyers in America
Fred Pritzker has been notified that he will again be listed in The Best Lawyers in America for his work in personal injury litigation.
Pain and Suffering
Rich Ruohonen recently chaired a legal seminar on obtaining compensation for pain and suffering in a personal injury case. Rich uses his knowledge, experience, and reputation to maximize recoveries for clients.
Medtronic Recall and Medtronic Lawsuit
FDA has annonced a Medtronic Spring Fidelis defibrillator lead recall. Two of our clients with defective Medtronic leads were shocked over twenty times before medical professionals were able to turn off the defibrillator.
Fleet Lawsuit
We are representing several people who experienced kidney failure (acute phosphate nephropathy) after use of Fleet Phospho-soda solution or Fleet Accu-Prep solution for bowel cleansing.
Ortho Evra Lawsuit: Ortho Evra Birth Control Patch
The Ortho Evra birth control patch has been linked to an increased risk of blood clots that can lead to pulmonary embolism, stroke and heart attack.
Trasylol Recall
Bayer has agreed to a marketing suspension of Trasylol, a drug used to control bleeding during heart surgery, pending detailed review of preliminary results from a Canadian study that suggested an increased risk for death.
Fentanyl Lawsuit and Fentanyl Recall
There have been a number of recalls regarding fentanyl due to the risk of a fentanyl overdose.
Fosamax and Osteonecrosis
Several cases of bisphosphonate-associated osteonecrosis of the jaw have been associated with the use of oral bisphosphonates, including Fosamax®, Actonel®, and other medications.
