Did you suffer as a result of taking Bravelle® or develop complications? Were you affected by this medication’s recall? If you’re among the many women who claimed Bravelle® did not work, you are not alone. We are here to help you stand up against those who are responsible for your injuries.
Ferring Pharmaeuticals, Inc. issued a recall after discovering an ineffective lot of Bravelle® was sold between between March 27, 2014 and October 15, 2015. If you underwent fertility treatment and were prescribed Bravelle® during this time, you may have subjected yourself unknowingly to an ineffective treatment.
Although Bravelle® is a fertility drug intended to help women who need medical assistance to get pregnant, the defective drug also placed women at risk to the serious side effects associated with fertility treatment. For many, the effects of this recall have seriously caused an emotional and financial burden among women going through this difficult type of treatment. You have every right to question how and why you were affected by the recall after taking Bravelle®.
Some of the more serious complications and risks women exposed themselves to include the following:
- lung problems
- blood clots
- ovarian hyperstimulation syndrome (OHSS)
We provide more information about Bravelle’s® complications and serious side effects on our Complications page. It’s important to understand why Bravelle® is prescribed and to whom, to see if you were affected by the recall.
If you or a loved one suffered as a result of taking Bravelle® and developed complications, call Avram Blair & Associates P.C. at (800) 692-0814. We can also help you determine if you have a case to file suit and recover compensation for the injuries you’ve suffered as a result of this drug.