Amisulpride (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Amisulpride" in English language version.

refsWebsite

Global rank English rank

26nih.gov

4^th place

23doi.org

2^nd place

13semanticscholar.org

11^th place

8^th place

3web.archive.org

1^st place

3fda.gov

447^th place

338^th place

2tga.gov.au

3,984^th place

2,622^nd place

2drugs.com

399^th place

333^rd place

2books.google.com

3^rd place

1in.gov.br

3,151^st place

5,932^nd place

1medicines.org.uk

3,823^rd place

2,387^th place

1medicinescomplete.com

low place

1archive.org

6^th place

1unc.edu

1,538^th place

1,042^nd place

1springer.com

274^th place

309^th place

1europa.eu

68^th place

117^th place

1psychiatrictimes.com

9,815^th place

7,507^th place

1lbpharma.us

low place

archive.org

Joint Formulary Committee (2013). British National Formulary (BNF) (65 ed.). London, UK: Pharmaceutical Press. ISBN 978-0-85711-084-8.

books.google.com

Haddad PM, Dursun S, Deakin B (2004). Adverse Syndromes and Psychiatric Drugs: A Clinical Guide. OUP Oxford. pp. 207–216. ISBN 978-0-19-852748-0.
Sacchetti E, Vita A, Siracusano A, Fleischhacker W (2013). Adherence to Antipsychotics in Schizophrenia. Springer Science & Business Media. p. 85. ISBN 978-8-84-702679-7.

doi.org

Rosenzweig P, Canal M, Patat A, Bergougnan L, Zieleniuk I, Bianchetti G (January 2002). "A review of the pharmacokinetics, tolerability and pharmacodynamics of amisulpride in healthy volunteers". Human Psychopharmacology. 17 (1): 1–13. doi:10.1002/hup.320. PMID 12404702. S2CID 23877366.
Caccia S (May 2000). "Biotransformation of post-clozapine antipsychotics: pharmacological implications". Clinical Pharmacokinetics. 38 (5): 393–414. doi:10.2165/00003088-200038050-00002. PMID 10843459. S2CID 68853079.
Noble S, Benfield P (December 1999). "Amisulpride: A Review of its Clinical Potential in Dysthymia". CNS Drugs. 12 (6): 471–483. doi:10.2165/00023210-199912060-00005. S2CID 71691764.
Pani L, Gessa GL (2002). "The substituted benzamides and their clinical potential on dysthymia and on the negative symptoms of schizophrenia". Molecular Psychiatry. 7 (3): 247–253. doi:10.1038/sj.mp.4001040. PMID 11920152.
Leucht S, Cipriani A, Spineli L, Mavridis D, Orey D, Richter F, et al. (September 2013). "Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis". Lancet. 382 (9896): 951–962. doi:10.1016/S0140-6736(13)60733-3. PMID 23810019. S2CID 32085212.
De Silva V, Hanwella R (April 2008). "Pharmaceutical patents and the quality of mental healthcare in low- and middle-income countries". The Psychiatrist. 32 (4): 121–23. doi:10.1192/pb.bp.107.015651.
Komossa K, Rummel-Kluge C, Hunger H, Schmid F, Schwarz S, Silveira da Mota Neto JI, et al. (January 2010). "Amisulpride versus other atypical antipsychotics for schizophrenia". The Cochrane Database of Systematic Reviews (1): CD006624. doi:10.1002/14651858.CD006624.pub2. PMC 4164462. PMID 20091599.
Solanki RK, Singh P, Munshi D (October–December 2009). "Current perspectives in the treatment of resistant schizophrenia". Indian Journal of Psychiatry. 51 (4): 254–260. doi:10.4103/0019-5545.58289. PMC 2802371. PMID 20048449.
Mouaffak F, Tranulis C, Gourevitch R, Poirier MF, Douki S, Olié JP, et al. (2006). "Augmentation strategies of clozapine with antipsychotics in the treatment of ultraresistant schizophrenia". Clinical Neuropharmacology. 29 (1): 28–33. doi:10.1097/00002826-200601000-00009. PMID 16518132. S2CID 29682562.
Nuss P, Hummer M, Tessier C (March 2007). "The use of amisulpride in the treatment of acute psychosis". Therapeutics and Clinical Risk Management. 3 (1): 3–11. doi:10.2147/tcrm.2007.3.1.3. PMC 1936283. PMID 18360610.
McKeage K, Plosker GL (2004). "Amisulpride: a review of its use in the management of schizophrenia". CNS Drugs. 18 (13): 933–956. doi:10.2165/00023210-200418130-00007. PMID 15521794. S2CID 9054960.
Natesan S, Reckless GE, Barlow KB, Nobrega JN, Kapur S (October 2008). "Amisulpride the 'atypical' atypical antipsychotic--comparison to haloperidol, risperidone and clozapine". Schizophrenia Research. 105 (1–3): 224–235. doi:10.1016/j.schres.2008.07.005. PMID 18710798. S2CID 11315672.
Moncrieff J (July 2006). "Does antipsychotic withdrawal provoke psychosis? Review of the literature on rapid onset psychosis (supersensitivity psychosis) and withdrawal-related relapse". Acta Psychiatrica Scandinavica. 114 (1): 3–13. doi:10.1111/j.1600-0447.2006.00787.x. PMID 16774655. S2CID 6267180.
Isbister GK, Balit CR, Macleod D, Duffull SB (August 2010). "Amisulpride overdose is frequently associated with QT prolongation and torsades de pointes". Journal of Clinical Psychopharmacology. 30 (4): 391–395. doi:10.1097/JCP.0b013e3181e5c14c. PMID 20531221. S2CID 205710487.
Joy JP, Coulter CV, Duffull SB, Isbister GK (August 2011). "Prediction of torsade de pointes from the QT interval: analysis of a case series of amisulpride overdoses". Clinical Pharmacology and Therapeutics. 90 (2): 243–245. doi:10.1038/clpt.2011.107. PMID 21716272. S2CID 26412012.
Levine M, Ruha AM (July 2012). "Overdose of atypical antipsychotics: clinical presentation, mechanisms of toxicity and management". CNS Drugs. 26 (7): 601–611. doi:10.2165/11631640-000000000-00000. PMID 22668123. S2CID 24628641.
Abbas AI, Hedlund PB, Huang XP, Tran TB, Meltzer HY, Roth BL (July 2009). "Amisulpride is a potent 5-HT7 antagonist: relevance for antidepressant actions in vivo". Psychopharmacology. 205 (1): 119–128. doi:10.1007/s00213-009-1521-8. PMC 2821721. PMID 19337725.
Maitre M, Ratomponirina C, Gobaille S, Hodé Y, Hechler V (April 1994). "Displacement of [3H] gamma-hydroxybutyrate binding by benzamide neuroleptics and prochlorperazine but not by other antipsychotics". European Journal of Pharmacology. 256 (2): 211–214. doi:10.1016/0014-2999(94)90248-8. PMID 7914168.
Blomme A, Conraux L, Poirier P, Olivier A, Koenig JJ, Sevrin M, Durant F, George P (2000). "Amisulpride, Sultopride and Sulpiride: Comparison of Conformational and Physico-Chemical Properties". Molecular Modeling and Prediction of Bioactivity. Springer US. pp. 404–405. doi:10.1007/978-1-4615-4141-7_97. ISBN 978-1-4613-6857-1.
Hopkins SC, Wilkinson S, Corriveau TJ, Nishikawa H, Nakamichi K, Loebel A, Koblan KS (September 2021). "Discovery of Nonracemic Amisulpride to Maximize Benefit/Risk of 5-HT7 and D2 Receptor Antagonism for the Treatment of Mood Disorders". Clinical Pharmacology and Therapeutics. 110 (3): 808–815. doi:10.1002/cpt.2282. PMC 8453756. PMID 33961287.
Grattan V, Vaino AR, Prensky Z, Hixon MS (August 2019). "Antipsychotic Benzamides Amisulpride and LB-102 Display Polypharmacy as Racemates, S Enantiomers Engage Receptors D₂ and D₃, while R Enantiomers Engage 5-HT₇". ACS Omega. 4 (9): 14151–14154. doi:10.1021/acsomega.9b02144. PMC 6714530. PMID 31497735.
Jethwa KD (2015). "Pharmacological management of antipsychotic-induced akathisia: An update and treatment algorithm". BJPsych Advances. 21 (5): 342–344. doi:10.1192/apt.bp.114.013797. S2CID 146670706.
Lecrubier Y, Azorin M, Bottai T, Dalery J, Garreau G, Lempérière T, et al. (2001). "Consensus on the Practical Use of Amisulpride, an Atypical Antipsychotic, in the Treatment of Schizophrenia". Neuropsychobiology. 44 (1): 41–46. doi:10.1159/000054913. PMID 11408792. S2CID 21103201.

drugs.com

"Amisulpride (Barhemsys) Use During Pregnancy". Drugs.com. 2 September 2020. Retrieved 24 September 2020.
"Amisulpride international". Drugs.com. 3 February 2020. Retrieved 26 February 2020.

europa.eu

ema.europa.eu

"Active substance: amisulpride" (PDF). 28 September 2017. EMA/658194/2017; Procedure no.: PSUSA/00000167/201701. Archived from the original (PDF) on 15 June 2018. Retrieved 26 February 2020.

fda.gov

accessdata.fda.gov

"Barhemsys (amisulpride) injection, for intravenous use" (PDF). U.S. Food and Drug Administration (FDA). February 2020. Retrieved 26 February 2020.
"Barhemsys: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Retrieved 26 February 2020.

fda.gov

"Drug Trials Snapshots: Barhemsys". U.S. Food and Drug Administration (FDA). 26 February 2020. Retrieved 27 March 2020. This article incorporates text from this source, which is in the public domain.

in.gov.br

Anvisa (31 March 2023). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 4 April 2023). Archived from the original on 3 August 2023. Retrieved 16 August 2023.

lbpharma.us

"Investor Presentation" (PDF). LB Pharmaceuticals. December 2022.

medicines.org.uk

"Amisulpride 100 mg Tablets - Summary of Product Characteristics (SmPC)". (emc). 5 July 2019. Archived from the original on 26 February 2020. Retrieved 26 February 2020.

medicinescomplete.com

Brayfield A, ed. (June 2017). "Amisulpride: Martindale: The Complete Drug Reference". MedicineComplete. Pharmaceutical Press. Retrieved 5 August 2017.

nih.gov

pubmed.ncbi.nlm.nih.gov

Rosenzweig P, Canal M, Patat A, Bergougnan L, Zieleniuk I, Bianchetti G (January 2002). "A review of the pharmacokinetics, tolerability and pharmacodynamics of amisulpride in healthy volunteers". Human Psychopharmacology. 17 (1): 1–13. doi:10.1002/hup.320. PMID 12404702. S2CID 23877366.
Caccia S (May 2000). "Biotransformation of post-clozapine antipsychotics: pharmacological implications". Clinical Pharmacokinetics. 38 (5): 393–414. doi:10.2165/00003088-200038050-00002. PMID 10843459. S2CID 68853079.
Pani L, Gessa GL (2002). "The substituted benzamides and their clinical potential on dysthymia and on the negative symptoms of schizophrenia". Molecular Psychiatry. 7 (3): 247–253. doi:10.1038/sj.mp.4001040. PMID 11920152.
Leucht S, Cipriani A, Spineli L, Mavridis D, Orey D, Richter F, et al. (September 2013). "Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis". Lancet. 382 (9896): 951–962. doi:10.1016/S0140-6736(13)60733-3. PMID 23810019. S2CID 32085212.
Komossa K, Rummel-Kluge C, Hunger H, Schmid F, Schwarz S, Silveira da Mota Neto JI, et al. (January 2010). "Amisulpride versus other atypical antipsychotics for schizophrenia". The Cochrane Database of Systematic Reviews (1): CD006624. doi:10.1002/14651858.CD006624.pub2. PMC 4164462. PMID 20091599.
Solanki RK, Singh P, Munshi D (October–December 2009). "Current perspectives in the treatment of resistant schizophrenia". Indian Journal of Psychiatry. 51 (4): 254–260. doi:10.4103/0019-5545.58289. PMC 2802371. PMID 20048449.
Mouaffak F, Tranulis C, Gourevitch R, Poirier MF, Douki S, Olié JP, et al. (2006). "Augmentation strategies of clozapine with antipsychotics in the treatment of ultraresistant schizophrenia". Clinical Neuropharmacology. 29 (1): 28–33. doi:10.1097/00002826-200601000-00009. PMID 16518132. S2CID 29682562.
Nuss P, Hummer M, Tessier C (March 2007). "The use of amisulpride in the treatment of acute psychosis". Therapeutics and Clinical Risk Management. 3 (1): 3–11. doi:10.2147/tcrm.2007.3.1.3. PMC 1936283. PMID 18360610.
McKeage K, Plosker GL (2004). "Amisulpride: a review of its use in the management of schizophrenia". CNS Drugs. 18 (13): 933–956. doi:10.2165/00023210-200418130-00007. PMID 15521794. S2CID 9054960.
Natesan S, Reckless GE, Barlow KB, Nobrega JN, Kapur S (October 2008). "Amisulpride the 'atypical' atypical antipsychotic--comparison to haloperidol, risperidone and clozapine". Schizophrenia Research. 105 (1–3): 224–235. doi:10.1016/j.schres.2008.07.005. PMID 18710798. S2CID 11315672.
Moncrieff J (July 2006). "Does antipsychotic withdrawal provoke psychosis? Review of the literature on rapid onset psychosis (supersensitivity psychosis) and withdrawal-related relapse". Acta Psychiatrica Scandinavica. 114 (1): 3–13. doi:10.1111/j.1600-0447.2006.00787.x. PMID 16774655. S2CID 6267180.
Isbister GK, Balit CR, Macleod D, Duffull SB (August 2010). "Amisulpride overdose is frequently associated with QT prolongation and torsades de pointes". Journal of Clinical Psychopharmacology. 30 (4): 391–395. doi:10.1097/JCP.0b013e3181e5c14c. PMID 20531221. S2CID 205710487.
Joy JP, Coulter CV, Duffull SB, Isbister GK (August 2011). "Prediction of torsade de pointes from the QT interval: analysis of a case series of amisulpride overdoses". Clinical Pharmacology and Therapeutics. 90 (2): 243–245. doi:10.1038/clpt.2011.107. PMID 21716272. S2CID 26412012.
Levine M, Ruha AM (July 2012). "Overdose of atypical antipsychotics: clinical presentation, mechanisms of toxicity and management". CNS Drugs. 26 (7): 601–611. doi:10.2165/11631640-000000000-00000. PMID 22668123. S2CID 24628641.
Abbas AI, Hedlund PB, Huang XP, Tran TB, Meltzer HY, Roth BL (July 2009). "Amisulpride is a potent 5-HT7 antagonist: relevance for antidepressant actions in vivo". Psychopharmacology. 205 (1): 119–128. doi:10.1007/s00213-009-1521-8. PMC 2821721. PMID 19337725.
Maitre M, Ratomponirina C, Gobaille S, Hodé Y, Hechler V (April 1994). "Displacement of [3H] gamma-hydroxybutyrate binding by benzamide neuroleptics and prochlorperazine but not by other antipsychotics". European Journal of Pharmacology. 256 (2): 211–214. doi:10.1016/0014-2999(94)90248-8. PMID 7914168.
Schoemaker H, Claustre Y, Fage D, Rouquier L, Chergui K, Curet O, et al. (January 1997). "Neurochemical characteristics of amisulpride, an atypical dopamine D2/D3 receptor antagonist with both presynaptic and limbic selectivity". The Journal of Pharmacology and Experimental Therapeutics. 280 (1): 83–97. PMID 8996185.
Hopkins SC, Wilkinson S, Corriveau TJ, Nishikawa H, Nakamichi K, Loebel A, Koblan KS (September 2021). "Discovery of Nonracemic Amisulpride to Maximize Benefit/Risk of 5-HT7 and D2 Receptor Antagonism for the Treatment of Mood Disorders". Clinical Pharmacology and Therapeutics. 110 (3): 808–815. doi:10.1002/cpt.2282. PMC 8453756. PMID 33961287.
Grattan V, Vaino AR, Prensky Z, Hixon MS (August 2019). "Antipsychotic Benzamides Amisulpride and LB-102 Display Polypharmacy as Racemates, S Enantiomers Engage Receptors D₂ and D₃, while R Enantiomers Engage 5-HT₇". ACS Omega. 4 (9): 14151–14154. doi:10.1021/acsomega.9b02144. PMC 6714530. PMID 31497735.
Lecrubier Y, Azorin M, Bottai T, Dalery J, Garreau G, Lempérière T, et al. (2001). "Consensus on the Practical Use of Amisulpride, an Atypical Antipsychotic, in the Treatment of Schizophrenia". Neuropsychobiology. 44 (1): 41–46. doi:10.1159/000054913. PMID 11408792. S2CID 21103201.

ncbi.nlm.nih.gov

Komossa K, Rummel-Kluge C, Hunger H, Schmid F, Schwarz S, Silveira da Mota Neto JI, et al. (January 2010). "Amisulpride versus other atypical antipsychotics for schizophrenia". The Cochrane Database of Systematic Reviews (1): CD006624. doi:10.1002/14651858.CD006624.pub2. PMC 4164462. PMID 20091599.
Solanki RK, Singh P, Munshi D (October–December 2009). "Current perspectives in the treatment of resistant schizophrenia". Indian Journal of Psychiatry. 51 (4): 254–260. doi:10.4103/0019-5545.58289. PMC 2802371. PMID 20048449.
Nuss P, Hummer M, Tessier C (March 2007). "The use of amisulpride in the treatment of acute psychosis". Therapeutics and Clinical Risk Management. 3 (1): 3–11. doi:10.2147/tcrm.2007.3.1.3. PMC 1936283. PMID 18360610.
Abbas AI, Hedlund PB, Huang XP, Tran TB, Meltzer HY, Roth BL (July 2009). "Amisulpride is a potent 5-HT7 antagonist: relevance for antidepressant actions in vivo". Psychopharmacology. 205 (1): 119–128. doi:10.1007/s00213-009-1521-8. PMC 2821721. PMID 19337725.
Hopkins SC, Wilkinson S, Corriveau TJ, Nishikawa H, Nakamichi K, Loebel A, Koblan KS (September 2021). "Discovery of Nonracemic Amisulpride to Maximize Benefit/Risk of 5-HT7 and D2 Receptor Antagonism for the Treatment of Mood Disorders". Clinical Pharmacology and Therapeutics. 110 (3): 808–815. doi:10.1002/cpt.2282. PMC 8453756. PMID 33961287.
Grattan V, Vaino AR, Prensky Z, Hixon MS (August 2019). "Antipsychotic Benzamides Amisulpride and LB-102 Display Polypharmacy as Racemates, S Enantiomers Engage Receptors D₂ and D₃, while R Enantiomers Engage 5-HT₇". ACS Omega. 4 (9): 14151–14154. doi:10.1021/acsomega.9b02144. PMC 6714530. PMID 31497735.

psychiatrictimes.com

Kaplan A (2004). "Psychotropic Medications Around the World". Psychiatric Times. 21 (5).

semanticscholar.org

api.semanticscholar.org

Rosenzweig P, Canal M, Patat A, Bergougnan L, Zieleniuk I, Bianchetti G (January 2002). "A review of the pharmacokinetics, tolerability and pharmacodynamics of amisulpride in healthy volunteers". Human Psychopharmacology. 17 (1): 1–13. doi:10.1002/hup.320. PMID 12404702. S2CID 23877366.
Caccia S (May 2000). "Biotransformation of post-clozapine antipsychotics: pharmacological implications". Clinical Pharmacokinetics. 38 (5): 393–414. doi:10.2165/00003088-200038050-00002. PMID 10843459. S2CID 68853079.
Noble S, Benfield P (December 1999). "Amisulpride: A Review of its Clinical Potential in Dysthymia". CNS Drugs. 12 (6): 471–483. doi:10.2165/00023210-199912060-00005. S2CID 71691764.
Leucht S, Cipriani A, Spineli L, Mavridis D, Orey D, Richter F, et al. (September 2013). "Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis". Lancet. 382 (9896): 951–962. doi:10.1016/S0140-6736(13)60733-3. PMID 23810019. S2CID 32085212.
Mouaffak F, Tranulis C, Gourevitch R, Poirier MF, Douki S, Olié JP, et al. (2006). "Augmentation strategies of clozapine with antipsychotics in the treatment of ultraresistant schizophrenia". Clinical Neuropharmacology. 29 (1): 28–33. doi:10.1097/00002826-200601000-00009. PMID 16518132. S2CID 29682562.
McKeage K, Plosker GL (2004). "Amisulpride: a review of its use in the management of schizophrenia". CNS Drugs. 18 (13): 933–956. doi:10.2165/00023210-200418130-00007. PMID 15521794. S2CID 9054960.
Natesan S, Reckless GE, Barlow KB, Nobrega JN, Kapur S (October 2008). "Amisulpride the 'atypical' atypical antipsychotic--comparison to haloperidol, risperidone and clozapine". Schizophrenia Research. 105 (1–3): 224–235. doi:10.1016/j.schres.2008.07.005. PMID 18710798. S2CID 11315672.
Moncrieff J (July 2006). "Does antipsychotic withdrawal provoke psychosis? Review of the literature on rapid onset psychosis (supersensitivity psychosis) and withdrawal-related relapse". Acta Psychiatrica Scandinavica. 114 (1): 3–13. doi:10.1111/j.1600-0447.2006.00787.x. PMID 16774655. S2CID 6267180.
Isbister GK, Balit CR, Macleod D, Duffull SB (August 2010). "Amisulpride overdose is frequently associated with QT prolongation and torsades de pointes". Journal of Clinical Psychopharmacology. 30 (4): 391–395. doi:10.1097/JCP.0b013e3181e5c14c. PMID 20531221. S2CID 205710487.
Joy JP, Coulter CV, Duffull SB, Isbister GK (August 2011). "Prediction of torsade de pointes from the QT interval: analysis of a case series of amisulpride overdoses". Clinical Pharmacology and Therapeutics. 90 (2): 243–245. doi:10.1038/clpt.2011.107. PMID 21716272. S2CID 26412012.
Levine M, Ruha AM (July 2012). "Overdose of atypical antipsychotics: clinical presentation, mechanisms of toxicity and management". CNS Drugs. 26 (7): 601–611. doi:10.2165/11631640-000000000-00000. PMID 22668123. S2CID 24628641.
Jethwa KD (2015). "Pharmacological management of antipsychotic-induced akathisia: An update and treatment algorithm". BJPsych Advances. 21 (5): 342–344. doi:10.1192/apt.bp.114.013797. S2CID 146670706.
Lecrubier Y, Azorin M, Bottai T, Dalery J, Garreau G, Lempérière T, et al. (2001). "Consensus on the Practical Use of Amisulpride, an Atypical Antipsychotic, in the Treatment of Schizophrenia". Neuropsychobiology. 44 (1): 41–46. doi:10.1159/000054913. PMID 11408792. S2CID 21103201.

springer.com

adisinsight.springer.com

"SEP 4199". AdisInsight. Springer Nature Switzerland AG.

tga.gov.au

ebs.tga.gov.au

"Australian Product Information – Solian (Amisulpride) Tablets And Solution". TGA eBS. Retrieved 10 May 2020.
"Solian tablets and solution product information" (PDF). TGA eBusiness Services. Sanofi-Aventis Australia Pty Ltd. 27 September 2019. Retrieved 26 February 2020.

unc.edu

pdsp.unc.edu

Roth BL, Driscol J. "PDSP K_i Database". Psychoactive Drug Screening Program (PDSP). University of North Carolina at Chapel Hill and the United States National Institute of Mental Health. Retrieved 14 August 2017.

web.archive.org

Anvisa (31 March 2023). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 4 April 2023). Archived from the original on 3 August 2023. Retrieved 16 August 2023.
"Amisulpride 100 mg Tablets - Summary of Product Characteristics (SmPC)". (emc). 5 July 2019. Archived from the original on 26 February 2020. Retrieved 26 February 2020.
"Active substance: amisulpride" (PDF). 28 September 2017. EMA/658194/2017; Procedure no.: PSUSA/00000167/201701. Archived from the original (PDF) on 15 June 2018. Retrieved 26 February 2020.