Bravelle Lyophilisate For Solution For Injection 75iu Drug Medication Dosage Information
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Bravelle: Lyophilisate for solution for injection (75IU)

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What is this Medicine?

UROFOLLITROPIN is a fertility medicine. It is used to stimulate the ovaries. This may increase the chance of pregnancy.

In-Depth Information

Bravelle 75units Powder for Injection

NDC: 555668505
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Hypogonadism, Oligospermia, Infertility

Storage Information
Reconstituted product should be used immediately. Discard unused portion
Protect from light
Store unreconstituted product in refrigerator or at room temperature (37 and 77 degrees F)
Bravelle 75units Powder for Injection

Reported Side Effects for Bravelle 75units Powder for Injection

Breast Pain Incidence:
2.0%*
Severity: MILD
Onset: DELAYED
Emotional Lability Incidence:
2.0-2.7%*
Severity: MILD
Onset: EARLY
Constipation Incidence:
2.0-2.7%*
Severity: MODERATE
Onset: DELAYED
Sinus Infection Incidence:
2.0%*
Severity: MILD
Onset: DELAYED
Labor Incidence:
2.7%*
Severity: MODERATE
Onset: EARLY
Loose Stools Incidence:
2.7%*
Severity: MILD
Onset: EARLY
Depression Incidence:
2.7%*
Severity: MODERATE
Onset: DELAYED
Dehydration Incidence:
2.7%*
Severity: MODERATE
Onset: DELAYED
Vomiting Incidence:
2.7%*
Severity: MILD
Onset: EARLY
Vaginal Discharge Incidence:
2.7%*
Severity: MILD
Onset: DELAYED
High Blood Pressure Incidence:
2.7%*
Severity: MODERATE
Onset: EARLY
Skin Rash Incidence:
2.7%*
Severity: MILD
Onset: EARLY
Exfoliative Dermatitis Incidence:
2.7%*
Severity: SEVERE
Onset: DELAYED
Vaginal Discharge Incidence:
2.7%*
Severity: MILD
Onset: DELAYED
Fever Incidence:
2.7%*
Severity: MILD
Onset: EARLY
Vaginal Bleeding Incidence:
2.7-8.6%*
Severity: MODERATE
Onset: DELAYED
Stomach Pain Incidence:
2.9-5.4%*
Severity: MILD
Onset: EARLY
Acne Incidence:
2.9%*
Severity: MILD
Onset: DELAYED
Injection Site Reaction Incidence:
4.0%*
Severity: MILD
Onset: RAPID
Hot Flashes Incidence:
4.0-5.7%*
Severity: MODERATE
Onset: EARLY
Ovarian Hyperstimulation Syndrome (OHSS) Incidence:
5.0-11.4%*
Severity: SEVERE
Onset: DELAYED
Upset Stomach Incidence:
5.7-8.7%*
Severity: MILD
Onset: EARLY
Pelvic Pain Incidence:
6.7%*
Severity: MILD
Onset: DELAYED
Headache Incidence:
8.1-12.7%*
Severity: MILD
Onset: EARLY
Enlarged Ovaries Incidence:
20.0%*
Severity: MODERATE
Onset: DELAYED
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class X - Adequate well-controlled or observational studies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities or risks. The use of the product is contraindicated in women who are or may become pregnant.

SECOND Trimester

Class X - Adequate well-controlled or observational studies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities or risks. The use of the product is contraindicated in women who are or may become pregnant.

THIRD Trimester

Class X - Adequate well-controlled or observational studies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities or risks. The use of the product is contraindicated in women who are or may become pregnant.

Lactation

Avoid - This drug is known to cause harm to infants when taken by nursing mothers.


Learning More About
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