Sir, Manini et al. express concerns about the algorithm that we developed for the management of cardiotoxicity in citalopram overdose. We respond to their comments as follows:In the algorithm we use “dose estimate” and not “ingested dose”. The difference between the dose amount reported (based on the patient history, tablet counts and other available information) and the dose amount estimated in the modelling ranged from 0 to 75 mg, i.e. the reported dose amount was acceptably reliable [1].Of the three published cases that the authors quote where patients ingested less than 600 mg [2, 3, 4], two did not have an abnormal QT based on the QT nomogram derived from Fossa et al. [5, 6]. Bazett\u27s correction was used in these two cases despite i...
Pharmacokinetic–pharmacodynamic (PKPD) analyses are complex and time consuming and many would believ...
Aims: To describe the pharmacokinetics and pharmacodynamics (PKPD) of escitalopram in overdose and i...
Fowler et al. (2007) state that the clopidogrel-oseltamivir interaction (in vivo) is remote because ...
I thank Lugassy et al for their interest in our study. However, they provide poor reasoning for cita...
We thank Greene et al for their comments on our study of citalopram overdoses. They raise a number o...
Design: Simulation study using a previously developed pharmacokinetic-pharmacodynamic (PKPD) model w...
Objective: To develop guidelines for the management of QT prolongation after citalopram overdose, in...
Megarbane et al. suggest in their letter that pharmacokinetic–pharmacodynamic (PKPD) analysis in ind...
To the Editor: We would like to comment on the article "A Fatal Case of Serotonin Syndrome afte...
Defining the pharmacokinetics of drugs in overdose is complicated. Deliberate self-poisoning is gene...
Abstract. A quantitative systems toxicology (QST) model for citalopram was established to simulate,...
Authors compared plasma concentrations of citalopram (CIT) enantiomers and their metabolites in pati...
Study objective: We determine whether single-dose activated charcoal (SDAC) administration after cit...
Background: The U.S. Food and Drug Administration (FDA) has stated that citalopram and escitalopram ...
pre-printWe appreciate the comments of Drs. Craig and Simpson and Drs. Mullins and Schwartz, and the...
Pharmacokinetic–pharmacodynamic (PKPD) analyses are complex and time consuming and many would believ...
Aims: To describe the pharmacokinetics and pharmacodynamics (PKPD) of escitalopram in overdose and i...
Fowler et al. (2007) state that the clopidogrel-oseltamivir interaction (in vivo) is remote because ...
I thank Lugassy et al for their interest in our study. However, they provide poor reasoning for cita...
We thank Greene et al for their comments on our study of citalopram overdoses. They raise a number o...
Design: Simulation study using a previously developed pharmacokinetic-pharmacodynamic (PKPD) model w...
Objective: To develop guidelines for the management of QT prolongation after citalopram overdose, in...
Megarbane et al. suggest in their letter that pharmacokinetic–pharmacodynamic (PKPD) analysis in ind...
To the Editor: We would like to comment on the article "A Fatal Case of Serotonin Syndrome afte...
Defining the pharmacokinetics of drugs in overdose is complicated. Deliberate self-poisoning is gene...
Abstract. A quantitative systems toxicology (QST) model for citalopram was established to simulate,...
Authors compared plasma concentrations of citalopram (CIT) enantiomers and their metabolites in pati...
Study objective: We determine whether single-dose activated charcoal (SDAC) administration after cit...
Background: The U.S. Food and Drug Administration (FDA) has stated that citalopram and escitalopram ...
pre-printWe appreciate the comments of Drs. Craig and Simpson and Drs. Mullins and Schwartz, and the...
Pharmacokinetic–pharmacodynamic (PKPD) analyses are complex and time consuming and many would believ...
Aims: To describe the pharmacokinetics and pharmacodynamics (PKPD) of escitalopram in overdose and i...
Fowler et al. (2007) state that the clopidogrel-oseltamivir interaction (in vivo) is remote because ...