Anonymous ID: cc71c9 Aug. 29, 2021, 5:13 a.m. No.14485177   🗄️.is 🔗kun   >>5481

>>14485109

How convenient, that they allegedly safeguard against 'severe illness and death.' That's the same prognosis as non vaxed have with regards to the virus and flu

Only certain people with underlying issues, have more severe cases or succumb to the illness.

But hey, it's just not quite the same, without the fear porn factor.

Anonymous ID: cc71c9 Aug. 29, 2021, 5:16 a.m. No.14485185   🗄️.is 🔗kun

>>14485120

>Anyone else feel like we’re being catfished?

 

Of course. Get ready to "be shown" just how all tragic events, were planned by the DS.

911, Katrina, Haiti etc.

 

You knew I was a SNAKE before you let ne in…

Anonymous ID: cc71c9 Aug. 29, 2021, 6:08 a.m. No.14485344   🗄️.is 🔗kun

>>14485292

 

NDA 50-742/S-024

NDA 50-742/S-025

Merck and Co., Inc.

Attention: Peter Kusma

Manager, Regulatory Affairs

P. O. Box 1000, UG2CD-48

North Wales, PA 19454-1099

Dear Mr. Kusma:

Please refer to your supplemental new drug applications submitted under section 505(b) of the Federal

Food, Drug, and Cosmetic Act for Stromectol™ (ivermectin), Tablets 3 mg as follows:

 

We acknowledge receipt of your submissions dated December 17, 2008 and April 22, 2009 for

NDA 50-742/S-024 and April 1, 2009 for NDA 50-742/S-025. Your submissions dated April 1, 2009

contained the final printed labeling for both supplements S-024 and S-025.

These “Changes Being Effected” supplemental new drug applications provide for revisions to the

formatting of the ADVERSE REACTIONS/Post-Marketing experience subsection of the package

insert and addition of Onchocerciasis/conjunctival hemorrhage (S-024) and addition of hepatitis (S025) to the same subsection of the package insert as follows (underlined text = addition, strikethrough

text = deletion):

The ADVERSE REACTIONS/Post-Marketing experience subsection is revised as follows:

Post-Marketing Experience

The following adverse reactions have been reported since the drug was registered overseas:

Onchocerciasis

Conjunctival hemorrhage

Post-Marketing Experience forAll Indications

The following adverse reactions have been reported since the drug was registered

overseas:Hhypotension (mainly orthostatic hypotension), worsening of bronchial asthma,

toxic epidermal necrolysis, Stevens-Johnson syndrome, seizures, hepatitis, elevation of liver

enzymes, and elevation of bilirubin.

 

We completed our review of these applications, as amended. These applications are approved,

effective on the date of this letter, for use as recommended in the agreed-upon labeling text for the

package insert submitted on April 1, 2009.

If you issue a letter communicating important information about this drug product (i.e., a “Dear Health

Care Professional” letter), we request that you submit a copy of the letter to this NDA and a copy to

the following address:

MEDWATCH

Food and Drug Administration

Suite 12B05

5600 Fishers Lane

 

Rockville, MD 20857

We remind you that you must comply with reporting requirements for an approved NDA

(21 CFR 314.80 and 314.81).

If you have any questions, call Judit Milstein, Regulatory Project Manager, at (301) 796-1600.

Sincerely,

{See appended electronic signature page}

Ozlem Belen, M.D., MPH

Deputy Director for Safety

Division of Special Pathogen and Transplant

Products

Office of Antimicrobial Products

Center for Drug Evaluation and Research

 

Link for above

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2009/050742s024,s025ltr.pdf

 

NDA 50-742/S-024 and S-025

Page 3

TABLETS

STROMECTOL®

(IVERMECTIN)

 

INDICATIONS AND USAGE

STROMECTOL is indicated for the treatment of the following infections:

Strongyloidiasis of the intestinal tract. STROMECTOL is indicated for the treatment of intestinal (i.e.,

nondisseminated) strongyloidiasis due to the nematode parasite Strongyloides stercoralis.

This indication is based on clinical studies of both comparative and open-label designs, in which 64-100% of

infected patients were cured following a single 200-mcg/kg dose of ivermectin. (See CLINICAL

PHARMACOLOGY, Clinical Studies.)

Onchocerciasis. STROMECTOL is indicated for the treatment of onchocerciasis due to the nematode

parasite Onchocerca volvulus.

This indication is based on randomized, double-blind, placebo-controlled and comparative studies conducted

in 1427 patients in onchocerciasis-endemic areas of West Africa. The comparative studies used

diethylcarbamazine citrate (DEC-C).

NOTE: STROMECTOL has no activity against adult Onchocerca volvulus parasites. The adult parasites

reside in subcutaneous nodules which are infrequently palpable. Surgical excision of these nodules

(nodulectomy) may be considered in the management of patients with onchocerciasis, since this procedure will

eliminate the microfilariae-producing adult parasites

 

Link to above

https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/050742s024s025lbl.pdf