Prescription drug attorney in Allentown

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✓ 98% Success Rate - Attorneys with a track record that shows they personally care about every case and go the extra mile every time.

✓ No upfront costs - we front all of the legal fees and get paid on performance. In fact, we don't get paid unless you win.

✓ We are local and we KNOW Pennsylvania's system - Just because a firm gets a license to practice law here and buy up a bunch of bill boards around town doesn't mean that they have real experience fighting cases in PA's legal system every day. We are a Allentown based firm with attorneys that focus on Pennsylvania injury cases. We eat, drink and breath this every day.

✓ We are not intimidated by litigation - We do not allow insurance carriers to strong arm, intimidate or stagnate claims. We will not hesitate to take them to court to fight for you when needed. 

✓ No shortcuts - we go the extra mile to make sure that you get the highest compensation possible rather than settling right away as many injury firms do.

 We focus on you, not on getting the most cases in town like the guys on the billboards.

✓ Proprietary methods of case management for your very best client experience and ensure greater odds of success compared to high volume, low-touch firms.

✓ Talk directly to your attorney instead of getting passed off on case managers (if you've ever been through a car accident case, you'll know how valuable this is).

✓ We're consistently rated 5 stars by clients and have over 450 5-star reviews for a reason.

✓ No cost consultations - we'll help you find out if you have a case. If you don't, we'll help point you in the right direction. Win-win.

✓ We get results without compromising service - It's not easy to find a firm that provides our brand of one-on-one service but which has the resources to get results that smaller practices may not be able to.

Defective drugs can cause serious and potentially life-threatening injuries to patients. When a drug manufacturer fails to properly test or adequately warn consumers of potential risks, they may be held liable for damages through a personal injury lawsuit. In such cases, the injured party may be entitled to compensation for medical expenses, lost wages, pain and suffering, and more.

The U.S. Food and Drug Administration (FDA) is responsible for regulating drugs in the United States. The agency may issue recalls for drugs that are found to be defective, unsafe, or otherwise pose a risk to consumers. There are three classes of recalls, based on the severity of the risk:

  • Class I Recall: This is the most serious type of recall and is issued when there is a reasonable probability that the use of or exposure to a drug will result in adverse health effects or death. Examples of drugs that have been subject to Class I recalls include those that are contaminated with dangerous substances or those that have been mislabeled with incorrect dosage information.
  • Class II Recall: This type of recall is issued when the use or exposure to a drug may cause temporary adverse side effects or potentially permanent effects. Examples of drugs that have been subject to Class II recalls include those that contain impurities or those that have been manufactured improperly.
  • Class III Recall: This is the least serious type of recall and is issued when exposure to a drug is not likely to cause adverse health issues but still warrants a recall. Examples of drugs that have been subject to Class III recalls include those with packaging or labeling errors.

While FDA recalls may serve as evidence in personal injury lawsuits, they are not always necessary to establish liability. In many cases, a drug manufacturer may be held liable for damages even if a recall was not issued.

Injuries resulting from defective drugs can vary widely depending on the drug and the patient. For example, a drug used to treat high blood pressure may cause heart attacks or strokes in some patients, while a drug used to treat depression may cause suicidal thoughts or actions. Injuries resulting from defective drugs may include:

  • Heart attacks or strokes
  • Liver or kidney damage
  • Birth defects
  • Internal bleeding
  • Suicidal thoughts or actions
  • Allergic reactions
  • Organ failure

In recent years, thousands of people have suffered from bad drugs and have pursued litigation. Some examples are: 

  • St. Jude Implantable Cardioverter Defibrillator
  • Prilosec
  • Prevacid/Prevacid 24-Hour
  • Risperdal
  • Taxotere
  • Nexium/Nexium 24-Hour
  • Ukoniq
  • Elmiron
  • Xeljanz
  • Tasigna
  • Zantac (Ranitidine)
  • Proton Pump Inhibitors
  • Zofran
  • Protonix
  • Onglyza
  • NSAIDs
  • Truvada
  • Pradaxa
  • Opioids
  • Uloric

Drug manufacturers, pharmacists, and physicians are accountable for ensuring the safety and effectiveness of prescription drugs. To gain FDA approval, drug manufacturers must conduct proper clinical testing and disclose all possible risks and warnings on the medication label. Pharmacists have the responsibility of dispensing precise dosages, as errors can have severe consequences. Physicians are required to prescribe the most suitable medication by taking into account the risks and benefits, as certain drugs can lead to long-term and serious side effects. If any of these parties failed to perform their duties and caused injury, a drug defect lawyer may be able to assist with obtaining compensation.

Pharmaceutical companies frequently promote their drugs for uses that are not approved by the FDA, which is known as off-label marketing. This may occur when a company discovers that a drug could potentially treat a condition that the FDA did not research and approve. However, this practice is hazardous, and if you have suffered harm due to off-label use, you may have the right to seek compensation through a defective drug lawsuit. The FDA approves drugs to be used in very specific ways, and promoting a drug for use in a manner that has not been approved is illegal. While physicians may legally prescribe drugs for off-label use, drug marketers are prohibited from promoting such usage.

Specialized medical and pharmacological expertise often plays an important role in personal injury cases involving defective drugs. Expert testimony from medical professionals may be necessary to establish the link between the drug and the injury, as well as to demonstrate the severity and impact of the injury on the patient.

If you or a loved one has been injured as a result of a defective drug, it is important to seek legal advice from an experienced personal injury attorney. An attorney can help you navigate the legal process, gather evidence, and pursue a claim for damages against the responsible party.

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