Elmiron–Drug Approved to Treat Pain Associated with Interstitial Cystitis–Linked to Blindness

In the 1990s, Janssen Pharmaceuticals introduced what was then considered a groundbreaking drug to treat the pain associated with interstitial cystitis, or IC. Unfortunately, those taking Elmiron didn’t know that in doing so, they were running the risk of going blind.

IC is a condition that affects millions of Americans each year and is more prevalent in women. IT’s a chronic condition that causes bladder pressure, pain, and pelvic pain. Hundreds of thousands of IC sufferers understandably jumped at the chance to control that pain and have been using Elmiron—also known as pentosan polysulfate sodium (PPS)—for decades, requiring dosage increases over the years.

Research presented at the American Academy of Ophthalmology in 2019 links that long-term use to ocular toxicity and irreversible vision damage.

They get put on these medications because it’s thought to have few side effects and few risks, and no one thinks about it again. And year after year, the number of pills they’re taking goes up and up.

Drs. Robin A. Vora, in an American Academy of Ophthalmology news release.

Elmiron causes pigmentary maculopathy, a condition that, according to the scientist researching it, is unique to Elmiron users. If you’re lucky enough to catch it in its early stages, the maculopathy damage may stop if you stop taking Elmiron. But, unfortunately, late stage maculopathy can lead to permanent vision loss. And at least one patient’s eye damage continued for years after stopping Elmiron.

These are the most common symptoms patients with pigmentary maculopathy have reported:

  • Areas of vision loss in the field of vision, paracentral scotoma
  • Difficult time adjusting to dim lighting or the dark
  • Having a hard time reading
  • Problems seeing objects that are close
  • Vision dimming

Lawsuits have been filed against Janssen Pharmaceuticals for failing to properly warn the public about the risk of pigmentary maculopathy and other vision problems. The plaintiffs in these lawsuits have alleged injuries including:

  • Blurred vision
  • Degenerative maculopathy
  • Halo vision
  • Macular retinopathy
  • Macular/pattern dystrophy
  • Maculopathy
  • Metamorphopsia
  • Pigmentary maculopathy
  • Reduced night vision
  • Retinal pigment epithelium atrophy
  • Retinopathy
  • Scotoma
  • Unilateral or bilateral blindness
  • Vision impairment
  • Vision loss

If you’ve taken Elmiron, you should seek an eye examination immediately and consult with your urologist on alternative treatment options. If you have been diagnosed with pigmentary maculopathy or are suffering from any of the above conditions and have taken Elmiron, contact a lawyer to discuss your options.

Wellements LLC Issues Allergy Alert On Undeclared Milk Allergen In Two Lots Of Iron Drops And Iron Drops Sample

Wellements LLC of Scottsdale, Arizona, is issuing a voluntary recall of two lots of its 1oz/30ml bottle of Iron Drops (UPC 729609000098) liquid Dietary Supplement and the sample version being Iron Drops Sample liquid Dietary Supplement because they may contain an undeclared milk allergen. People who

Source: Food and Drugs Administration--Recalls/Safety Alerts

Wellements LLC Issues Allergy Alert On Undeclared Milk Allergen In Two Lots Of Iron Drops And Iron Drops Sample

Wellements LLC of Scottsdale, Arizona, is issuing a voluntary recall of two lots of its 1oz/30ml bottle of Iron Drops (UPC 729609000098) liquid Dietary Supplement and the sample version being Iron Drops Sample liquid Dietary Supplement because they may contain an undeclared milk allergen. People who

Source: Food and Drugs Administration--Recalls/Safety Alerts

Allergy Alert for Undeclared Egg In Kouign-Amann Pastries Issued By Select Whole Foods Market Stores In Seven States

Whole Foods Market is voluntarily recalling Kouign-amann pastries in 35 stores across Colorado, Kansas, Missouri, Nebraska, New Mexico, Texas and Utah due to undeclared eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if the

Source: FDA Food Safety Recalls RSS Feed

Allergy Alert for Undeclared Tree Nut (Almond) In Chantilly Key Lime Tartlets Issued By Whole Foods Market Stores In Five States

Whole Foods Market is voluntarily recalling Chantilly Key Lime Tartlets from stores in Connecticut, Maine, Massachusetts, New Hampshire and Rhode Island due to an undeclared tree nut (almond) allergen. People who have a food allergy or severe sensitivity to almonds run the risk of serious or life-th

Source: FDA Food Safety Recalls RSS Feed

Real Clean Distribuciones SA de CV Issues Voluntary Nationwide Recall of Four Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol)

La Loma, Tlalnepantla, Mexico, Real Clean Distribuciones SA de CV is voluntarily recalling all lots it manufactured within expiry of the following brand names of hand sanitizers: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures,

Source: Food and Drugs Administration--Recalls/Safety Alerts

UpSpring LLC Issues Allergy Alert On Undeclared Milk In ” UpSpring Baby Iron + Immunity “

UpSpring LLC of Austin, TX is recalling one batch of its 60 ml dark brown glass bottles sold in cartons of "UpSpring Baby Iron + Immunity" dietary supplements because it may contain undeclared milk allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-thr

Source: Food and Drugs Administration--Recalls/Safety Alerts

Willis Electric Recalls Home Accents Holiday Artificial Christmas Trees Due to Burn Hazard; Sold Exclusively at Home Depot

The Christmas tree’s foot-pedal controller can overheat, posing a burn hazard.

Source: Recall List

Willis Electric Recalls Home Accents Holiday Artificial Christmas Trees Due to Burn Hazard; Sold Exclusively at Home Depot

The Christmas tree’s foot-pedal controller can overheat, posing a burn hazard.

Source: Recall List

Fresenius Kabi Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine

Fresenius Kabi USA is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg / mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to the possibility of a trace amount of lidocaine present in these two lots and our investig

Source: Food and Drugs Administration--Recalls/Safety Alerts