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Transplant

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News
07/17/2024
Jolynn Tumolo
After a patient receives a solid organ transplant, long-term nutrition management is key to navigate potential adverse events from immunosuppressive therapies needed to prevent rejection, according to an invited review article published in...
After a patient receives a solid organ transplant, long-term nutrition management is key to navigate potential adverse events from immunosuppressive therapies needed to prevent rejection, according to an invited review article published in...
After a patient receives a solid...
07/17/2024
Pharmacy Learning Network
News
05/30/2024
Jolynn Tumolo
Dr Reddy’s Laboratories Inc. is recalling 1176 bottles of sirolimus tablets for failing to meet impurities/degradation specifications.
Dr Reddy’s Laboratories Inc. is recalling 1176 bottles of sirolimus tablets for failing to meet impurities/degradation specifications.
Dr Reddy’s Laboratories Inc. is...
05/30/2024
Pharmacy Learning Network
News
01/26/2022
Liz Szabo
Amid changing guidelines from the Centers for Disease Control and Prevention, pharmacies are denying fourth COVID-19 shots to patients with weakened immune systems.
Amid changing guidelines from the Centers for Disease Control and Prevention, pharmacies are denying fourth COVID-19 shots to patients with weakened immune systems.
Amid changing guidelines from...
01/26/2022
Pharmacy Learning Network
News
08/17/2014
Compared to standard basiliximab-based induction therapy, treatment based on alemtuzumab reduces rejection in kidney transplant recipients, according to findings from a UK-based study.
Compared to standard basiliximab-based induction therapy, treatment based on alemtuzumab reduces rejection in kidney transplant recipients, according to findings from a UK-based study.
Compared to standard...
08/17/2014
Pharmacy Learning Network

News
07/17/2024
Jolynn Tumolo
After a patient receives a solid organ transplant, long-term nutrition management is key to navigate potential adverse events from immunosuppressive therapies needed to prevent rejection, according to an invited review article published in...
After a patient receives a solid organ transplant, long-term nutrition management is key to navigate potential adverse events from immunosuppressive therapies needed to prevent rejection, according to an invited review article published in...
After a patient receives a solid...
07/17/2024
Pharmacy Learning Network
News
05/30/2024
Jolynn Tumolo
Dr Reddy’s Laboratories Inc. is recalling 1176 bottles of sirolimus tablets for failing to meet impurities/degradation specifications.
Dr Reddy’s Laboratories Inc. is recalling 1176 bottles of sirolimus tablets for failing to meet impurities/degradation specifications.
Dr Reddy’s Laboratories Inc. is...
05/30/2024
Pharmacy Learning Network
News
01/26/2022
Liz Szabo
Amid changing guidelines from the Centers for Disease Control and Prevention, pharmacies are denying fourth COVID-19 shots to patients with weakened immune systems.
Amid changing guidelines from the Centers for Disease Control and Prevention, pharmacies are denying fourth COVID-19 shots to patients with weakened immune systems.
Amid changing guidelines from...
01/26/2022
Pharmacy Learning Network
News
08/17/2014
Compared to standard basiliximab-based induction therapy, treatment based on alemtuzumab reduces rejection in kidney transplant recipients, according to findings from a UK-based study.
Compared to standard basiliximab-based induction therapy, treatment based on alemtuzumab reduces rejection in kidney transplant recipients, according to findings from a UK-based study.
Compared to standard...
08/17/2014
Pharmacy Learning Network
News
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for clomiphene citrate due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug Administration (FDA) has issued a Class II recall for clomiphene citrate due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
News
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for bortezomib injections due to a lack of sterility assurance, affecting 11 400 vials.
The US Food and Drug Administration (FDA) has issued a Class II recall for bortezomib injections due to a lack of sterility assurance, affecting 11 400 vials.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
News
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for methohexital sodium injections due to the product’s failure to meet impurities/degradation specifications, affecting 4284 vials.
The US Food and Drug Administration (FDA) has issued a Class II recall for methohexital sodium injections due to the product’s failure to meet impurities/degradation specifications, affecting 4284 vials.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
PharmLaw
07/15/2026
Hannah Musick
The Federal Trade Commission's (FTC) proposed settlement with CVS Caremark would require significant changes to pharmacy benefit manager (PBM) rebate practices, transparency, formulary management, and pharmacy contracting, signaling evolving...
The Federal Trade Commission's (FTC) proposed settlement with CVS Caremark would require significant changes to pharmacy benefit manager (PBM) rebate practices, transparency, formulary management, and pharmacy contracting, signaling evolving...
The Federal Trade Commission's...
07/15/2026
Pharmacy Learning Network
News
07/09/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for combination extended-release capsules of dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate due to a...
The US Food and Drug Administration (FDA) has issued a Class II recall for combination extended-release capsules of dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate due to a...
The US Food and Drug...
07/09/2026
Pharmacy Learning Network
News
07/09/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for Synjardy XR (empagliflozin and metformin hydrochloride) tablets due to Current Good Manufacturing Practice (CGMP) deviations, affecting 560 bottles.
The US Food and Drug Administration (FDA) has issued a Class II recall for Synjardy XR (empagliflozin and metformin hydrochloride) tablets due to Current Good Manufacturing Practice (CGMP) deviations, affecting 560 bottles.
The US Food and Drug...
07/09/2026
Pharmacy Learning Network
News
07/09/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for Imuldosa (ustekinumab-srlf) injections due to a lack of sterility assurance, affecting 326 vials.
The US Food and Drug Administration (FDA) has issued a Class II recall for Imuldosa (ustekinumab-srlf) injections due to a lack of sterility assurance, affecting 326 vials.
The US Food and Drug...
07/09/2026
Pharmacy Learning Network
PharmLaw
07/08/2026
Grace Taylor, MS, MA
Former executives of Done Global were sentenced to federal prison after convictions in a multimillion-dollar scheme involving unlawful telehealth prescribing of Adderall and health care fraud, according to the US Department of Justice.
Former executives of Done Global were sentenced to federal prison after convictions in a multimillion-dollar scheme involving unlawful telehealth prescribing of Adderall and health care fraud, according to the US Department of Justice.
Former executives of Done Global...
07/08/2026
Pharmacy Learning Network
News
07/02/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for lacosamide tablets, 100 mg, due to the presence of foreign tablets, affecting 31 392 bottles.
The US Food and Drug Administration (FDA) has issued a Class II recall for lacosamide tablets, 100 mg, due to the presence of foreign tablets, affecting 31 392 bottles.
The US Food and Drug...
07/02/2026
Pharmacy Learning Network
News
07/02/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for sensipar (cinacalcet) tablets due to Current Good Manufacturing Practice (CGMP) deviations, affecting 9565 bottles.
The US Food and Drug Administration (FDA) has issued a Class II recall for sensipar (cinacalcet) tablets due to Current Good Manufacturing Practice (CGMP) deviations, affecting 9565 bottles.
The US Food and Drug...
07/02/2026
Pharmacy Learning Network