FAQ About Unsafe Medications

It is crucial to stay informed about the actions taken by manufacturers and distributors in response to product recalls. In the case of the recalled eye drops, here are the steps that have been taken:

• EzriCare Recall: Aru Pharma Inc., the company that formulated EzriCare artificial... read more?

As a personal injury attorney, it's essential to guide clients on the appropriate steps to take if they have a recalled eye drop product. If you find yourself in this situation, here's what you should do:

• Stop using the product immediately: If you have a recalled eye drop product,... read more?

As a personal injury attorney, it's important to understand the reasons behind product recalls, particularly those that may have significant health implications for our clients. In the case of the recent eye drop recalls, several key factors have led to these products being removed... read more?

As a personal injury attorney, it's crucial to stay informed about product recalls that may impact our clients' health and well-being. In this case, we have recently seen a series of eye drop recalls that warrant attention:

• EzriCare Artificial Tear Drops: These eye drops were... read more?

If you believe you have suffered injuries or complications due to using the recalled eye drops, it's essential to take the following steps to protect your health and legal rights:

1. Seek immediate medical attention: Consult a healthcare professional as soon as possible to address your... read more?

If you have been affected by the recent eye drop recall, you may be wondering whether you can file a lawsuit to seek compensation for your injuries or damages. The short answer is yes, you may be able to pursue a legal claim if you have been harmed by the recalled eye drops. However, it's... read more?

Understanding the timeline for filing a lawsuit related to the eye drop recall is essential for protecting your legal rights. While the time limits for filing a lawsuit can vary by state, here are some general guidelines to help you understand the process:

• Statute of Limitations:... read more?

If you believe you have been harmed by the recalled eye drops and are considering pursuing a lawsuit, it's natural to wonder what type of compensation you might be able to receive if your case is successful. As an attorney with extensive experience in personal injury law, I can tell you that... read more?

If you have been harmed by the recalled eye drops, The Ruth Law Team can provide you with valuable support and guidance throughout the legal process. Our experienced attorneys understand the complexities of personal injury law and can help you navigate your case to pursue the... read more?

If you or a loved one has been affected by the eye drop recall, you may be wondering if you will have to pay any upfront fees for legal representation. The good news is that most personal injury attorneys, including The Ruth Law Team, work on a contingency fee basis. This means that you... read more?

In 1985, Elmiron was granted an FDA orphan drug designation, which is defined as “those intended for the safe and effective treatment, diagnosis, or prevention of rare diseases/disorders that affect fewer than 200,000 people in the US or that affect more than 200,000 persons but are not expected... read more?

Interstitial cystitis (IC) is a chronic condition typically (but not always) found in women.  It causes bladder pressure, bladder pain, and sometimes pelvic pain.  There is currently no known cure for the condition, and the pain may negatively affect a person’s day-to-day life.  Elmiron is one of the only drugs developed to treat IC.

NDMA stands for Ni-nitrosodimethylamine.  NDMA is classified as a probable human carcinogen, which is a substance that causes cancer.  It is not only usd to manufacture rocket fuel, but it is also used to induce tumors in animals for laboratory experiments.  The FDA’s daily allowable limit is 96ng.  

On September... read more?

Valisure LLC and ValisureRX LLC conducted tests, finding very high levels of NDMA in all lots of ranitidine tested.  Valisure tests showed the NDMA concentration in a patient’s urine to be more than 15,000 times higher than the California drinking water limit.  A Stanford study studied NDMA... read more?

Zantac has been completely recalled, so you are no longer able to purchase it at the store. Doctors will no longer prescribe Zantac. Talk to your doctor before discontinuing use of any medication, and speak to him or her about any alternatives that may be available to you.