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Generic "Clomid" is a drug of considerable pharmacologic potency. With careful selection and proper management of the patient, Generic "Clomid" has been demonstrated to be a useful therapy for the anovulatory patient desiring pregnancy.
Generic "Clomid" is capable of interacting with estrogen-receptor-containing tissues, including the hypothalamus, pituitary, ovary, endometrium, vagina, and cervix.

Active Ingredients: Clomiphene
Inactive Ingredients: corn starch, lactose, magnesium stearate, pregelatinized cornstarch, and sucrose.

Generic "Clomid" is indicated for patients with hormonal stimulation deficiencies who are not capable of producing follicles and releasing eggs in ovulation. Generic "Clomid" stimulates the release of hormones to aid a woman to ovulate. Clomid may also be used for other purposes aside from the ones mentioned here.

Treatment of the selected patient should begin with a low dose, 50 mg daily (1 tablet) for 5 days. The dose should be increased only in those patients who do not ovulate in response to cyclic 50 mg. A low dosage or duration of treatment course is particularly recommended if unusual sensitivity to pituitary gonadotropin is suspected, such as in patients with polycystic ovary syndrome.

Generic "Clomid" is contraindicated in patients with a known hypersensitivity or allergy to clomiphene citrate or to any of its ingredients.
Generic "Clomid" should not be administered during pregnancy. Generic "Clomid" may cause fetal harm in animals. Although no causative evidence of a deleterious effect of Generic "Clomid" therapy on the human fetus has been established, there have been reports of birth anomalies which, during clinical studies, occurred at an incidence within the range reported for the general population. To avoid inadvertent Generic "Clomid" administration during early pregnancy, appropriate tests should be utilized during each treatment cycle to determine whether ovulation occurs. The patient should be evaluated carefully to exclude pregnancy, ovarian enlargement, or ovarian cyst formation between each treatment cycle. The next course of Generic "Clomid" therapy should be delayed until these conditions have been excluded.
Generic "Clomid" therapy is contraindicated in patients with liver disease or a history of liver dysfunction
Generic "Clomid" is contraindicated in patients with ovarian cysts or enlargement not due to polycystic ovarian syndrome.
Generic "Clomid" is contraindicated in patients with uncontrolled thyroid or adrenal dysfunction or in the presence of an organic intracranial lesion such as pituitary tumor
Generic "Clomid" is contraindicated in patients with abnormal uterine bleeding of undetermined origin

Generic "Clomid" should be taken at a regular interval as per doctor's orders. However, if a dose of Generic "Clomid" is missed, you should call your doctor for advice on what to do next.

Toxic effects accompanying acute overdosage of Generic "Clomid" have not been reported. Signs and symptoms of overdosage as a result of the use of more than the recommended dose during Generic "Clomid" therapy include nausea, vomiting, vasomotor flushes, visual blurring, spots or flashes, scotomata, ovarian enlargement with pelvic or abdominal pain.

Allergic Reactions is likely to occur on susceptible patients. Allergic reactions are manifested by the following symptoms: Hives, Swelling of lips, mouth and tongue, Rashes, Closing of throat.
Other side effects also include: Blurred vision, Headache, Abnormal uterine bleeding, Breast discomfort and tenderness, Pelvic pain, Swelling of pelvic area.
Other side effects may also be likely to occur and you should inform your doctor on what to do when they become intolerable or bothersome.

There are no known dangerous drug interactions of Generic "Clomid" with other drugs but it is still wise to inform your doctor of the drugs you are taking may they be prescription or non-prescription drugs as other drugs may not be advised for simultaneous intake with Generic "Clomid".