Ovidrel

Ovidrel

choriogonadotropin alfa

Manufacturer:

PT. Merck Tbk
Concise Prescribing Info
Contents
Choriogonadotropin α (Recombinant DNA)
Indications/Uses
Dosage/Direction for Use
By SC inj. Women undergoing superovulation prior to assisted reproductive techniques eg, in vitro fertilisation (IVF) 250 mcg SC 24-48 hr after the last administration of an FSH or hMG prep. Anovulatory or oligo-ovulatory women 250 mcg SC 24-48 hr after optimal follicular growth stimulation is achieved. The patient is recommended to have coitus on the day of & the day after inj.
Contraindications
Hypothalamic & pituitary tumours; ovarian enlargement or cyst due to reasons other than polycystic ovarian disease; gynaecological haemorrhage of unknown aetiology; ovarian, uterine or mammary carcinoma; extrauterine pregnancy in the previous 3 mth; active thromboembolic disorders. Pregnancy & lactation.
Special Precautions
Hypothyroidism, adrenocortical deficiency, hyperprolactinemia, pituitary or hypothalamic tumours, clinically significant systemic diseases where pregnancy could exacerbate the condition.
Adverse Reactions
Local reactions or inj site pain, headache, mild to severe ovarian hyperstimulation syndrome. Vomiting/nausea, abdominal pain.
MIMS Class
Trophic Hormones & Related Synthetic Drugs
ATC Classification
G03GA08 - choriogonadotropin alfa ; Belongs to the class of gonadotropins. Used as ovulation stimulants.
Presentation/Packing
Form
Ovidrel inj 250 mcg/0.5 mL
Packing/Price
(pen) 1's (Rp638,348/boks)
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