The only FDA-approved oral solution of granisetron, GRANISOL, is now available to patients enrolled in Medicaid
CALIFON, NJ - April 6, 2011 - PediatRx, Inc. (OTCBB: PEDX) announced
that the U.S. Centers for Medicare and Medicaid Services (CMS) recently notified
state Medicaid agencies to include PediatRx’s GRANISOL, NDC 52547-0801-30, in their
list of reimbursed products. CMS funds the Medicaid and State Children Health Insurance
Programs jointly with state governments. These programs provide health insurance,
including prescription drug coverage, to over 40 million low-income families,* and
this number is expected to grow with the implementation of health care reform legislation.
Dr. Cameron Durrant, founder of PediatRx, said, "We are delighted to have reached
an agreement with CMS to include PediatRx's GRANISOL on the list of reimbursed products
for Medicaid. This means that individual state Medicaid programs can now add GRANISOL
to their formularies, enabling patients enrolled in Medicaid access to the only
once-daily oral solution of granisetron."
CMS provided in its notice to PediatRx two effective dates: an optional effective
date of March 17, 2011, and a mandatory effective date of July 1, 2011. States can
begin covering GRANISOL at their option any time between these two dates. Patients
and health care providers can contact their state Medicaid program to find out if
GRANISOL has been added at the current time. See
http://www.cms.gov/MedicaidDrugRebateProgram/downloads/drugcon.pdf
Durrant continued, "We are acutely aware of the financial pressures on patients,
including those who are not eligible for government-sponsored healthcare programs
or are uninsured or underinsured. That is why we developed a co-pay assistance program,
GRANI Cares, to support GRANISOL for eligible patients."
For patients who are not enrolled in Medicaid or Medicare, visit GRANI Cares:
http://www.121hm.com/offers/granisol
For disclaimer information, visit:
http://www.121hm.com/offers/granisol/tandc.html
About GRANISOL
Granisetron is indicated for the prevention of:
- Nausea and vomiting associated with initial and repeat courses of emetogenic cancer therapy, including high-dose cisplatin.
- Nausea and vomiting associated with radiation, including total body irradiation and fractionated abdominal radiation.
For full prescribing information, visit: http://www.pediatrx.com/products/pdf/granisol_pi.pdf
Selected Safety Information
- GRANISOL is contraindicated in patients with known hypersensitivity to the drug or any of its components.
- QT prolongation has been reported with granisetron. Therefore, GRANISOL Oral Solution should be used in caution with patients with pre-existing arrhythmias or cardiac conduction disorders, as this might lead to clinical consequences. Patients with cardiac disease, on cardio-toxic chemotherapy, with concomitant electrolyte abnormalities and/or on concomitant medications that prolong the QT interval are particularly at risk.
- Safety and effectiveness in pediatric patients have not been established.
- The most common side effects observed with administration of granisetron were headache, asthenia, constipation, diarrhea, dyspepsia, and abdominal pain.
*2009 U.S. Census Bureau.
About PediatRx Inc.
PediatRx, Inc. (www.pediatrx.com) is a hospital
specialty pharmaceutical company which focuses on treatments for patients suffering
from serious conditions requiring hospitalization. PediatRx trades on the OTCBB
under the ticker symbol PEDX.
Forward-Looking Statements
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are projections of events, revenues, income, future economic, research, development,
reformulation, product performance or management's plans and objectives for future
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of terminology such as "may", "should", "anticipates", "believes", "expects", "intends",
"forecasts", "plans", "future", "strategy", or words of similar meaning. Forward-looking
statements in this press release include those concerning PediatRx’s intention to
acquire and/or license, and become the sole marketer in the United States, of other
FDA-approved, branded prescription drugs as well as reformulate certain compounds
as more appropriate forms. While these forward-looking statements and any assumptions
upon which they are based are made in good faith and reflect current judgment regarding
the direction of the business operations of PediatRx, actual results will almost
always vary, sometimes materially, from any estimates, predictions, projections,
assumptions or other future performance suggested in this press release. These statements
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including the risk that PediatRx cannot execute its business plan for lack of capital
or other resources, distribution, partnering or licensing/acquisition opportunities,
as well as the risks described in the periodic disclosure documents filed on EDGAR
by PediatRx, copies of which are also available on the company’s website. Any of
these risks could cause PediatRx or its industry's actual results, levels of activity,
performance or achievements to be materially different from those expressed or implied
by the forward-looking statements in this press release. Except as required by applicable
law, including the securities laws of the United States, PediatRx does not intend
to update any of the forward-looking statements to conform these statements to actual
results.
Futher Information
PediatRx Inc.
Research & Business Development
Email: info@pediatrx.com
Shareholder Relations
+1 908 975 0753
Email: ir@pediatrx.com