Sildoo D Combipack contains Silodosin. Sildoo D Combipack uses:

Sildoo D Combipack , a selective alpha-1 adrenergic receptor antagonist, is indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH). Sildoo D Combipack is not indicated for the treatment of hypertension.

Brand Name: Sildoo D Combipack
Generic: Silodosin
Weight: 8.0 Mg
Type: Capsule
Therapeutic Class: BPH/ Urinary retention/ Urinary incontinence
Price: 280.5
Last Updated: 2020-11-19 18:15:00


Sildoo D Combipack contains Silodosin 8.0 Mg. Sildoo D Combipack doses

The recommended dose is Sildoo D Combipack 8 mg orally once daily with a meal. 4 mg capsules taken orally once daily with a meal for those with moderate renal impairment (CrCl 30-50 mL/min).


Side Effects

Most common adverse reactions are retrograde ejaculation, dizziness, diarrhea, orthostatic hypotension, headache, nasopharyngitis and nasal congestion.


Sildoo D Combipack is a selective antagonist of post-synaptic alpha-1 adrenoreceptors, which are located in the human prostate, bladder base, bladder neck, prostatic capsule and prostatic urethra. Blockade of these alpha-1 adrenoreceptors can cause smooth muscle in these tissues to relax, resulting in an improvement in urine flow and a reduction in BPH symptoms.


Postural hypotension with or without symptoms (e.g. dizziness) may develop when beginning Sildoo D Combipack treatment. Sildoo D Combipack should not be used in combination with other alpha-blocker. Inform patients planning cataract surgery to notify their ophthalmologist that they are taking Sildoo D Combipack because of the possibility of Intraoperative Floppy Iris Syndrome (IFIS)


Strong P-glycoprotein inhibitors (e.g., cyclosporine): Co-administration may increase plasma Sildoo D Combipack concentration. Concomitant use of PDE5 inhibitors with alpha-blockers including Sildoo D Combipack can potentially cause symptomatic hypotension.

Pregnancy Lactation use

Pregnancy Category B. Sildoo D Combipack is not indicated for use in women. An embryo/fetal study in rabbits showed decreased maternal body weight at 200 mg/kg/day (approximately 13-25 times the maximum recommended human exposure or MRHE of Sildoo D Combipack via AUC). No statistically significant teratogenicity was observed at this dose. Sildoo D Combipack was not teratogenic when administered to pregnant rats during organogenesis at 1000 mg/kg/day (estimated to be approximately 20 times the MRHE). No maternal or fetal effects were observed at this dose. Rats and rabbits do not produce glucuronidated Sildoo D Combipack , which is present in human serum at approximately 4 times the level of circulating Sildoo D Combipack and which has similar pharmacological activity to Sildoo D Combipack . No effects on physical or behavioral development of offspring were observed when rats were treated during pregnancy and lactation at up to 300 mg/kg/day.


Patients with severe renal & hepatic impairment, concomitant administration with strong Cytochrome P450 3A4 (CYP3A4) inhibitors (e.g., ketoconazole, clarithromycin, itraconazole, ritonavir) and patients with a history of hypersensitivity to Sildoo D Combipack .

Special Warning

Pediatric patients: Sildoo D Combipack is not indicated for use in pediatric patients. 

Geriatric use: In double-blind, placebo-controlled, 12-week clinical studies of Sildoo D Combipack , 259 (55.6%) were under 65 years of age, 207 (44.4%) patients were 65 years of age and over, while 60 (12.9%) patients were 75 years of age and over. Orthostatic hypotension was reported in 2.3% of Sildoo D Combipack patients < 65 years of age (1.2% for placebo), 2.9% of Sildoo D Combipack patients > 65 years of age (1.9% for placebo), and 5.0% of patients > 75 years of age (0% for placebo). There were otherwise no significant differences in safety or effectiveness between older and younger patients.

Renal impairment: Sildoo D Combipack is contra-indicated in patients with severe renal impairment (CCr <30 mL/min). In patients with moderate renal impairment (CCr 30-50 mL/min), the dose should be reduced to Sildoo D Combipack 4 mg once daily taken with a meal. No dosage adjustment is needed in patients with mild renal impairment (CCr 50-80 mL/min).

Hepatic impairment: Sildoo D Combipack has not been studied in patients with severe hepatic impairment (Child-Pugh score > 10) and is therefore contra-indicated in these patients. No dosage adjustment is needed in patients with mild or moderate hepatic impairment.

Acute Overdose

Sildoo D Combipack was evaluated at doses of up to 48 mg/day in healthy male subjects. The dose-limiting adverse event was postural hypotension. Should overdose of Sildoo D Combipack lead to hypotension, support of the cardiovascular system is of first importance. Restoration of blood pressure and normalization of heart rate may be accomplished by maintaining the patient in the supine position. If this measure is inadequate, administration of intravenous fluid should be considered. If necessary, vasopressors could be used, and renal function should be monitored and supported as needed. Dialysis is unlikely to be of significant benefit since Sildoo D Combipack is highly (97%) protein bound.

Interaction with other Medicine


Storage Condition

Store in a cool and dry place, protected from light.

Sildoo D Combipack Capsule price in India 280.5