Cialis Tablets (Tadalafil Tablets)

Side Effects

Most common Cialis (Tadalafil Tablets) side effects with an incidence rate of greater than or equal to 2% include headache, dyspepsia, back pain, myalgia, nasal congestion, flushing, and pain in limb.

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Side Effects

The following side effects occurred in less than 2% of the patients during Cialis clinical trials: Body as a Whole — asthenia, face edema, fatigue, pain

Cardiovascular — angina pectoris, chest pain, hypotension, myocardial infarction, postural hypotension, palpitations, syncope, tachycardia

Digestive — abnormal liver function tests, dry mouth, dysphagia, esophagitis, gastritis, GGTP increased, loose stools, nausea, upper abdominal pain, vomiting, gastroesophageal reflux disease, hemorrhoidal hemorrhage, rectal hemorrhage

Musculoskeletal — arthralgia, neck pain

Nervous — dizziness, hypesthesia, insomnia, paresthesia, somnolence, vertigo

Side Effects

The following side effects occurred in less than 2% of the patients during Cialis clinical trials: Renal and Urinary — renal impairment

Respiratory — dyspnea, epistaxis, pharyngitis

Skin and Appendages — pruritus, rash, sweating

Ophthalmologic — blurred vision, changes in color vision, conjunctivitis (including conjunctival hyperemia), eye pain, lacrimation increase, swelling of eyelids Otologic — sudden decrease or loss of hearing, tinnitus Urogenital — erection increased, spontaneous penile erection

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Overdose

Single doses up to 500 mg have been given to healthy subjects, and multiple daily doses up to 100 mg have been given to patients.

Adverse events observed were similar to those seen at lower doses. In cases of Cialis tablets overdose, standard supportive measures should be adopted as required.

Hemodialysis contributes negligibly to Tadalafil elimination. URL:https://www.clearskypharmacy.biz/cialis-tablets.html

Tadalafil Tablets During Pregnancy

Cialis (Tadalafil tablets) has been classified by the US FDA as Pregnancy Category B. There are no data regarding the use of Tadalafil tablets in pregnant women to inform any drug-associated risks for adverse developmental outcomes. During animal reproduction studies, no adverse developmental effects were observed with oral administration of Tadalafil to pregnant rats or mice during organogenesis at exposures up to 11 times the maximum recommended human dose (MRHD) of 20mg/day.

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