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INTRODUCTION ABOUT KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY

KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY contains Sildenafil which belongs to the group of medicines called PhosphodiesSterase type 5 (PDE 5) inhibitors. It helps in relaxing the blood vessels and allows more blood flow to the penis.

Avoid taking heavy meals while taking KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY, as it could delay the onset of action. Before taking KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY, inform your doctor if you have any liver, kidney, or heart problems. You must also inform your doctor if you have pulmonary arterial hypertension (PAH) and taking medications to manage it.

KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY is not intended for use in women. It is also not suitable for use in children and adolescents (below 18 years). Inform your doctor if you experience any painful and prolong erection after taking KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY. The most common side effects of taking KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY are flushing, headache, dizziness, blurred vision and muscle pain. Consult your doctor if any of the side effect troubles you.

How much to take?

The clinical trials were conducted in 20 participants who were candidates for sex with native or variant of the mening of Bengal union, India. The participants were randomly divided into 2 groups: group1 received KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY for 2 weeks, group 2 received KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY for 4 weeks, and group3 received KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY for 4 weeks.

How old to take KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY?

The clinical trials were conducted in 20 participants who were randomly divided into 2 groups: group1 received KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY for 2 weeks, group2 received KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY for 4 weeks, and group3 received KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY for 4 weeks.

How do I take KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY?

Take KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY as directed by your doctor.

How much to take

The clinical trials were conducted in 20 participants who were determined to have erectile dysfunction by their physicians. In group 1, the mean age was 71.6 years group 2. The mean duration of erections was 18.6 minutes in group 1 and 26.2 minutes in group 2.

Taking KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY?

Do not take KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY if you are allergic to Sildenafil, to any of the ingredients in KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY, or to any of the other ingredients in this medicine.

Kamagra FX PEPPERMINT FLAVOUR ORAL JELLY has been reported in the U. S. in association with prescribe it.Cautions and Side Effects

Precautions

KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY can trigger dizziness, lightheadedness, blurred vision, and muscle pain. Consult your doctor if any of these symptoms worsen your condition.

KAMAGRA FX PEPPERMINT FLAVOUR ORAL JELLY is also reported to cause flushing, headache, nausea, and stomach pain. Inform your doctor if you have any heart problems.

Product description

Product name:KAMAGRA ORAL JELLY

Company name:

DIN:06585946

Status:Marketed

Status date:2017-12-24

Active ingredient(s)	Strength
SILDENAFIL	100 MG

Resources

Click on a resource to visit a page with more information. You may be taken away from this page to a different Government of Canada website.

For consumers

Resource	Description
The Product Monograph is a scientific document that describes the properties, claims, indications and conditions of use of the product and contains any other information that may be required for optimal, safe and effective use. The Product Monograph includes three sections: Part I: Health Professional Information; Part II: Scientific Information; and Patient Medication Information
Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.

For health care professionals

Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals.

For researchers

After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

All resources

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