Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Sildenafil citrate
Drug ID BADD_D02019
Description In eliciting its mechanism of action, sildenafil ultimately prevents or minimizes the breakdown of cyclic guanosine monophosphate (cGMP) by inhibiting cGMP specific phosphodiesterase type 5 (PDE5) [F3850, F3853, F3856, F3859, F3883, F3886, L5611, L5614]. The result of doing so allows cGMP present in both the penis and pulmonary vasculature to elicit smooth muscle relaxation and vasodilation that subsequently facilitates relief in pulmonary arterial hypertension and the increased flow of blood into the spongy erectile tissue of the penis that consequently allows it to grow in size and become erect and rigid [F3850, F3853, F3856, F3859, F3883, F3886, L5611, L5614]. Interestingly enough, it is precisely via this mechanism why sildenafil was at first researched as a potential treatment for angina - or chest pain associated with inadequate blood flow to the heart - before being serendipitously indicated for treating erectile dysfunction in the late 1980s [A175732]. Nevertheless, it is because of this mechanism that sildenafil is also indicated for treating pulmonary arterial hypertension but is also additionally notorious for interacting with various anti-anginal or anti-hypertensive agents to develop potentially rapid, excessive, and/or fatal hypotensive crises [A175579, A175582, A175654]. Regardless, sildenafil, among a variety of other similar or related PDE5 inhibitors, has become a common and effective treatment for erectile dysfunction and since its formal approval for medical use in the public in 1998 [A175732], continues to see millions of prescriptions written for it internationally. Although the medication has historically been most popularly recognized as Pfizer's brand name Viagra, sildenafil is currently available generically and even as a non-prescription over the counter medication in some countries [L5656].
Indications and Usage Sildenafil is a phosphodiesterase-5 (PDE5) inhibitor that is predominantly employed for two primary indications: (1) the treatment of erectile dysfunction [A175582, L5611, F3853, F3856, F3886]; and (2) treatment of pulmonary hypertension, where: a) the US FDA specifically indicates sildenafil for the treatment of pulmonary arterial hypertension (PAH) (WHO Group I) in adults to improve exercise ability and delay clinical worsening [F3850]. The delay in clinical worsening was demonstrated when sildenafil was added to background epoprostenol therapy [F3850]. Studies establishing effectiveness were short-term (12 to 16 weeks), and included predominately patients with New York Heart Association (NYHA) Functional Class II-III symptoms and idiopathic etiology (71%) or associated with connective tissue disease (CTD) (25%) [F3850]; b) the Canadian product monograph specifically indicates sildenafil for the treatment of primary pulmonary arterial hypertension (PPH) or pulmonary hypertension secondary to connective tissue disease (CTD) in adult patients with WHO functional class II or III who have not responded to conventional therapy [F3859]. In addition, improvement in exercise ability and delay in clinical worsening was demonstrated in adult patients who were already stabilized on background epoprostenol therapy [F3859]; and c) the EMA product information specifically indicates sildenafil for the treatment of adult patients with pulmonary arterial hypertension classified as WHO functional class II and III, to improve exercise capacity [F3883]. Efficacy has been shown in primary pulmonary hypertension and pulmonary hypertension associated with connective tissue disease [F3883]. The EMA label also indicates sildenafil for the treatment of pediatric patients aged 1 year to 17 years old with pulmonary arterial hypertension [F3883]. Efficacy in terms of improvement of exercise capacity or pulmonary hemodynamics has been shown in primary pulmonary hypertension and pulmonary hypertension associated with congenital heart disease [F3883].
Marketing Status approved; investigational
ATC Code G04BE03
DrugBank ID DB00203
KEGG ID D02229
MeSH ID D000068677
PubChem ID 135413523
TTD Drug ID Not Available
NDC Product Code 0069-0336; 0069-0338; 65015-652; 68981-001; 59762-0035; 80425-0304; 12658-0585; 61281-1500; 63275-9892; 55150-166; 70954-168; 75834-241; 75834-272; 49452-7528; 50379-0001; 67835-5042; 72375-0001; 70771-1668; 62512-0038; 62991-2556; 0904-6671; 47621-005; 69097-903; 71205-657; 72205-059; 12658-0483; 0069-4210; 69575-4002; 71052-067; 59762-0034; 59762-0036; 70710-1716; 0069-4200; 0069-4220; 65015-861; 51672-4231; 59651-420; 67877-648; 38779-2950; 46144-320; 51927-5067; 65691-0063; 65862-696; 65977-0028; 73377-082; 27808-163; 55154-4307; 71205-721; 71205-795; 0069-4190; 13668-185; 43353-345; 75834-240; 10695-017; 12658-0586; 42185-7050; 51552-1352
UNII BW9B0ZE037
Synonyms Sildenafil Citrate | Citrate, Sildenafil | 1-((3-(6,7-Dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo(4,3-d)pyrimidin-5-yl)-4-ethoxyphenyl)sulfonyl)-4-methylpiperazine citrate | NCX-911 | NCX 911 | NCX911 | Revatio | Sildenafil | UK 92480-10 | UK 92480 10 | UK 9248010 | UK-92,480-10 | UK 92,480 10 | Homosildenafil | Hydroxyhomosildenafil | Viagra | Acetildenafil | Sildenafil Lactate | Lactate, Sildenafil | Sildenafil Nitrate | Nitrate, Sildenafil | Desmethyl Sildenafil | Sildenafil, Desmethyl | Desmethylsildenafil
Chemical Information
Molecular Formula C28H38N6O11S
CAS Registry Number 171599-83-0
SMILES CCCC1=NN(C2=C1N=C(NC2=O)C3=C(C=CC(=C3)S(=O)(=O)N4CCN(CC4)C)OCC)C.C(C(=O)O)C(CC(= O)O)(C(=O)O)O
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Blindness06.02.10.003; 17.17.01.003---
Cardiovascular disorder02.11.01.010; 24.03.02.009---
Cerebral haemorrhage17.08.01.003; 24.07.04.001---
Cerebrovascular disorder17.08.02.002; 24.03.05.002---
Deafness04.02.01.001---
Death08.04.01.001--
Diarrhoea07.02.01.001--
Dyspepsia07.01.02.001--
Dyspnoea02.11.05.003; 22.02.01.004--
Epistaxis22.04.03.001; 24.07.01.005--
Erythema23.03.06.001---
Eye haemorrhage06.07.02.001; 12.02.02.012; 24.07.05.002---
Flushing08.01.03.025; 23.06.05.003; 24.03.01.002--
Gastritis07.08.02.001--
Headache17.14.01.001--
Hypertension24.08.02.001--
Hypotension24.06.03.002--
Insomnia17.15.03.002; 19.02.01.002--
Myalgia15.05.02.001--
Myocardial infarction02.02.02.007; 24.04.04.009--
Nasal congestion22.04.04.001--
Nausea07.01.07.001--
Oedema08.01.07.006; 14.05.06.010---
Oedema peripheral02.05.04.007; 08.01.07.007; 14.05.06.011--
Pain in extremity15.03.04.010--
Paraesthesia17.02.06.005; 23.03.03.094--
Priapism21.03.01.005; 24.04.12.007---
Pulmonary haemorrhage22.12.01.009; 24.07.01.016--
Pyrexia08.05.02.003--
Retinal haemorrhage06.10.01.001; 24.07.05.003---
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