Kariva Side Effects, Overdose and Pregnancy Information

Kariva is used to prevent pregnancy, regulate menstrual periods as well as in the treatment of acne in women 15 and older. Kariva is a synthetic form of female sex hormones produced naturally in the body, progestin, and estrogen. Kariva curbs the pituitary glands activity thus hindering ovulation; alter the mucus at the cervix opening to prevent sperm from entering, and their variable levels play a vital role in fertility in women. Kariva for acne is taken just as it would be for contraception. Contraceptive drugs like Kariva are associated with risks. These risks increase in women over age 35, smokers and who have hypertension. Main ingredients in Kariva are Estrogen (low dose) and Progestin (high dose).

Kariva Side Effects

Kariva side effects include abdominal pain, vaginal discharge, acne, fluid retention, bloating, blood clots, chest pain, hair loss, headache, heart attack, and high blood pressure. Other Kariva side effects may include kidney problem, migraine, leg pain, nausea, sex drive changes, skin discoloration, stroke, vomiting, and weight gain or loss.

Kariva Side Effects Reporting


If you experience any Kariva side effects not mentioned above you should report it to your primary health care provider or FDA 1-800-FDA-1088 in the United States, Health Canada 1-866-225-0709 in Canada, MHRA 020 3080 6000 in UK, or TGA 1800 020 653 in Australia.

Kariva Overdose


Symptoms of Kariva overdose may include nausea, vomiting, and withdrawal bleeding. In case of Kariva overdose, seek medical attention right away. If you miss a dose of Kariva, take it as soon as you can. However, if it is just about time for your next dose, skip the one you forgot and go on with your regular schedule. Never take a double dose of Kariva.

KARIVA WARNING


Avoid using contraceptives including Kariva if you are or might be pregnant.

Avoid smoking as it enhances the risk of heart-related side effects in women who use oral contraceptives like Kariva. The risk is even greater in women over 35.

Avoid using Kariva if you have had an allergic reaction to any oral contraceptives.

Avoid Kariva if you are a migraine sufferer.

Avoid taking Kariva if you or someone in your family has ever had breast cancer or cancer of the reproductive system or liver problems.

Avoid Kariva if you have or ever had a stroke, heart disease, liver disease, chest pain, or blood clots.

Avoid Kariva if you have had pregnancy related jaundice or jaundice resulting from previous use of any oral contraceptives.

Avoid Kariva if you have experienced abnormal vaginal bleeding.



KARIVA CAUTION



Kariva should be used with caution if you are:

-Over 40

-Smoker

-Have liver, heart, gallbladder, kidney, or thyroid disease

-Have high blood pressure

-High cholesterol

-Diabetes

-Epilepsy

-Asthma

-Porphyria

-Obese

-Stroke or heart attack in the past

-Depression

-Family history of breast cancer or other cancers

-Kariva does not protect against HIV (AIDS), or other STDs.

-If you experience abdominal pain, contact your physician right away.

-In rare cases, oral contraceptives like Kariva may cause benign liver tumors.

KARIVA INTERACTION


Check with your physician before combining Kariva with the following:

Acetaminophen/ Paracetamol

Amitriptyline

Antibiotics

Ascorbic acid (Vitamin C)

Aspirin

Atorvastatin (anti-cholesterol drugs)

Barbiturates

Blood thinners

Carbamazepine

Chloramphenicol

Clofibrate

Clomipramine

Copper supplements

Cyclosporine

Diazepam

Doxepin

Fluconazole

Glipizide

Griseofulvin

HIV drugs

Imipramine

Propranolol

Insulin

Lorazepam

Metoprolol

Modafinil

Morphine

Oxazepam

Phenylbutazone

Phenytoin

Prednisolone

Prednisone

Primidone

Propranolol

Rifabutin

Rifampin

Sulfonamides

Temazepam

Tetracycline

Theophylline

Topiramate

Troleandomycin

Valium

Herbs like Black Cohosh, Milk Thistle, and St. John's Wort.

KARIVA DOSES


Consult your physician or the instructions in the drug package. For maximum effectiveness, Kariva tablets must be taken exactly as prescribed and at intermissions not exceeding 24 hours.
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