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| STABILITIES, COMPATIBILITIES RELATED ARTICLES |
| Title (Click for Details) |
Vol/Issue |
Page |
| Basics of Compounding: Implementing United States Pharmacopeia Chapter <795> Pharmaceutical Compounding--Nonsterile Preparations, Part 3 |
Vol. 15 No. 6 |
488 |
| Physiochemical Stability of Diluted Trastuzumab Infusion Solutions in Polypropylene Infusion Bags |
Vol. 15 No. 6 |
515 |
| Study of Microbiological Safety of 25 Oncology Drugs After Multiple Uses in Aseptic Conditions |
Vol. 15 No. 5 |
428 |
| Stability of Clopidogrel in Three Extemporaneously Compounded Oral Liquid Preparations |
Vol. 15 No. 5 |
435 |
| Preparation and Characterization of a New Alternative Formulation of Sodium p-aminosalicylate |
Vol. 15 No. 4 |
344 |
| Stability of Ertapenem in an Elastomeric Infusion Device |
Vol. 15 No. 3 |
252 |
| Stability of Verapamil Hydrochloride in SyrSpend SF Compared to Sorbitol Containing Syrup and Suspending Vehicles |
Vol. 15 No. 3 |
255 |
| Compatibility of Parenteral Furosemide with Seventeen Secondary Drugs Used in Standard Concentrations |
Vol. 15 No. 3 |
259 |
| Drug Compatibility and Stability in Dextrose vs Saline |
Vol. 15 No. 3 |
190 |
| Basics of Compounding: Basics of Compounding with Complex Organic Molecules |
Vol. 15 No. 3 |
234 |
| Basics of Compounding: Basics of Compounding with Inorganic Salts |
Vol. 15 No. 2 |
146 |
| Nifedpine in Compounded Oral and Topical Preparations |
Vol. 15 No. 2 |
166 |
| Stability of Droperidol 0.625 mg/mL Diluted with 0.9% Sodium Chloride Injection and Stored in Polypropylene Syringes |
Vol. 15 No. 2 |
170 |
| Maillard Reactions in Pharmaceutical Formulations and Human Health |
Vol. 15 No. 1 |
32 |
| Stability of Midazolam Intranasal Formulation for the Treatment of Status Epilepticus in Dogs |
Vol. 15 No. 1 |
74 |
| Chemical Stability of Brompheniramine Maleate in an Oral Liquid Dosage Form |
Vol. 15 No. 1 |
78 |
| Stability of Venlafaxine Immediate-Release Suspensions |
Vol. 15 No. 1 |
81 |
| PreScription: Compounding with Manufactured Products |
Vol. 14 No. 6 |
448 |
| Stability of Methimazole in Poloxamer Lecithin Organogel to Determine Beyond-Use Date |
Vol. 14 No. 6 |
522 |
| Quality Control and Physical and Chemical Stability of Hydrocortisone Oral Suspension: An Interlaboratory Study |
Vol. 14 No. 5 |
430 |
| Stability and Compatibility of Reconstituted Caspofungin in Select Elastomeric Infusion Device |
Vol. 14 No. 5 |
436 |
| Hygrometers and Thermohygrometers: Environmental Monitoring Ensures the Potency and Stability of Compounding Agents |
Vol. 14 No. 4 |
284 |
| Evaluation of Extemporaneous Oral Itraconazole Suspensions by Dissolution Profiles Mapping |
Vol. 14 No. 4 |
342 |
| Compatibility and Stability of Cefotaxine, Vancomycin, and Ciprofloxacin in Antibiotic Lock Solutions Containing Heparin |
Vol. 14 No. 4 |
346 |
| Basics of Compounding: Considerations for Implementing USP Chapter <797> -- Sterile Preparations, Part 19: Storage and Beyond-Use Dating, Maintaining Sterility, Purity, and Stability of Dispensed and Distributed Compounded Sterile Preparations |
Vol. 14 No. 3 |
232 |
| Compounding Rifampin Suspensions with Improved Injectability for Nasogastric Enteral Feeding Tube Administration |
Vol. 14 No. 3 |
250 |
| Developing a Tretinoin Oral Liquid for Patients Who Cannot Take Capsules |
Vol. 14 No. 2 |
118 |
| Chemical Stability of Hydromorphone Hydrochloride in Patient-Controlled Analgesia Injector |
Vol. 14 No. 2 |
160 |
| Chemical Stability of Hydrocortisone in Humco Simple Syrup and Ora-Sweet Vehicle |
Vol. 14 No. 1 |
76 |
| Evaluation of a Simple Method for Visual Detection of Microprecipitates in Blends of Parenteral Drug Solutions Using a Focussed (Tyndall) Light Beam |
Vol. 14 No. 1 |
78 |
| Stability of Oseltamivir Phosphate in SyrSpend SF, Cherry Syrup, and SyrSpend SF (For Reconstitution) |
Vol. 14 No. 1 |
82 |
| An Overview of United States Pharmacopeia Chapter <795> and American Society of Health-System Pharmacists Guidelines for Nonsterile Compounding |
Vol. 13 No. 6 |
525 |
| Stability of Preoperative Cataract Surgery Gel in Polycarbonate Syringes |
Vol. 13 No. 6 |
564 |
| Chemical Stability of Scopolamine Hydrobromide Nasal Solution |
Vol. 13 No. 5 |
438 |
| Chemical Stability of Amitriptyline Hydrochloride in Oral Liquid Dosage Forms |
Vol. 13 No. 5 |
445 |
| Chemical Stability of Extemporaneously Compounded Omeprazole Formulations: A Comparison of Two Methods of Compounding |
Vol. 13 No. 3 |
250 |
| Stability of Pergolide Mesylate Oral Liquid at Room Temperature |
Vol. 13 No. 3 |
254 |
| Drug Compatibility with a New Generation of VISIV Polyolefin Infusion Solution Containers |
Vol. 13 No. 2 |
162 |
| Stability of Low-Concentration Ceftazidime in 0.9% Sodium Chloride Injection and Balanced Salt Solutions in Plastic Syringes Under Various Storage Conditions |
Vol. 13 No. 2 |
166 |
| Stability of Melatonin in an Extemporaneously Compounded Sublingual Solution and Hard Gelatin Capsule |
Vol. 13 No. 2 |
170 |
| Identifying the Criteria of a Valid Stability Study |
Vol. 13 No. 1 |
32 |
| Compatibility and Stability of Palonosetron Hydrochloride and Propofol During Simulated Y-Site Administration |
Vol. 13 No. 1 |
78 |
| Testing the Long-Term Stability of Vancomycin Ophthalmic Solution |
Vol. 12 No. 5 |
456 |
| Compatibility and Stability of Palonosetron Hydrochloride with Lactated Ringer's, Hetastarch in Lactated Electrolyte, and Mannitol Injections During Simulated Y-Site Administration |
Vol. 12 No. 5 |
460 |
| Chemical Stability of Admixtures Combining Ziconotide with Fentanyl or Sufentanil During Simulated Intrathecal Administration |
Vol. 12 No. 5 |
463 |
| Quality-Control Analytical Methods: Overview of Beyond-Use Dating for Compounded Sterile Preparations |
Vol. 12 No. 6 |
524 |
| Physical Compatibility and Chemical Stability of a Concentrated Solution of Atropine Sulfate (2 mg/mL) for Use as an Antidote in Nerve Agent Casualties |
Vol. 12 No. 6 |
550 |
| Chemical Stability of Admixtures Containing Ziconotide 25 mcg/mL and Morphine Sulfate 10 mg/mL or 20 mg/mL During Simulated Intrathecal Administration |
Vol. 12 No. 6 |
553 |
| Stability of Metronidazole Benzoate in SyrSpend SF One-Step Suspension System |
Vol. 12 No. 6 |
558 |
| Basics of Compounding: Considerations for Implementing United States Pharmacopeia Chapter <797> Pharmaceutical Compounding--Sterile Preparations, Part 8; Stability and Beyond-Use Dating |
Vol. 12 No. 4 |
344 |
| Chemical Stability of Perphenazine in Two Commercially Available Vehicles for Oral Liquid Dosage Forms |
Vol. 12 No. 4 |
372 |
| Physical and Chemical Stability of Palonosetron Hydrochloride with Glycopyrrolate and Neostigmine During Simulated Y-Site Administration |
Vol. 12 No. 4 |
368 |
| Chemical Stability of Naltrexone Hydrochloride Injection |
Vol. 12 No. 3 |
274 |
| Dilution and Compounding of Ziconotide for Intrathecal Administration |
Vol. 12 No. 3 |
200 |
| Compatibility of Caspofungin Acetate Injection with Other Drugs During Simulated Y-Site Coadministration |
Vol. 12 No. 3 |
276 |
| Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm! |
Vol. 12 No. 2 |
130 |
| Compatibility and Stability of Palonosetron Hydrochloride with Four Neuromuscular Blocking Agents During Simulated Y-Site Administration |
Vol. 12 No. 2 |
156 |
| Chemical Stability of Tramadol Hydrochloride Injection |
Vol. 12 No. 2 |
161 |
| Pharmaceutical Development of Enteric-Release Hard Gelatin Capsules in the Compounding Setting |
Vol. 12 No. 2 |
163 |
| Compatibility and Stability of Palonosetron Hydrochloride with Gentamicin, Metronidazole, or Vancomycin During Simulated Y-Site Administration |
Vol. 12 No. 2 |
170 |
| Quality-Control Analytical Methods: Stability Versus Potency Testing: The Madness is in the Method |
Vol. 12 No. 1 |
50 |
| Room Temperature Stability of Injectable Succinylcholine Dichloride |
Vol. 12 No. 1 |
83 |
| Palonosetron Hydrochloride Compatibility and Stability with Three Beta-Lactam Antibiotics During Simulated Y-Site Administration |
Vol. 11 No. 6 |
520 |
| Zinc Content of Commercial Diluents Widely Use in Drug Admixtures Prepared for Intravenous Infusion |
Vol. 11 No. 5 |
426 |
| Chemical Stability of Cyproheptadine Hydrochloride in an Oral Liquid Dosage Form |
Vol. 11 No. 4 |
347 |
| Chemical Stability of Hydrocortisone in an Oral Liquid Dosage Form without Suspending Agents |
Vol. 11 No. 3 |
259 |
| Stability of Oseltamivir in Various Extemporaneous Liquid Preparations |
Vol. 11 No. 2 |
164 |
| Pediatric Oral Formulations: A Continual Challenge |
Vol. 11 No. 1 |
17 |
| Sevelamer Suspension in Children with End-Stage Renal Disease |
Vol. 11 No. 1 |
20 |
| Chemical Stability of Desonide in Ear Drops |
Vol. 11 No. 1 |
79 |
| Physical and Chemical Stability of Palonosetron with Metoclopramide and Promethazine During Simulated Y-Site Administration |
Vol. 11 No. 1 |
82 |
| Temozolomide Stability in Extemporaneously Compounded Oral Suspensions |
Vol. 10 No. 5 |
396 |
| Chemical Stability of Pyridoxine Hydrochloride 100-mg/mL Injection, Preservative Free |
Vol. 10 No. 4 |
318 |
| Physical Assessments of Lipid Injectable Emulsions via Microscopy: A Comparison to Methods Proposed in the United States Pharmacopeia Chapter <729> |
Vol. 10 No. 4 |
309 |
| Stability of Memantine in an Extemporaneously Prepared Oral Liquid |
Vol. 10 No. 4 |
316 |
| Compatibility of Micafungin Injection with Other Drugs During Simulated Y-Site Co-administration |
Vol. 10 No. 3 |
230 |
| Physical and Chemical Stability of Palonosetron Hydrochloride with Dacarbazine and with Methylprednisolone Sodium Succinate During Simulated Y-Site Administration |
Vol. 10 No. 3 |
234 |
| Chemical Stability of Diphenhydramine Hydrochloride from an Elixir and Lidocaine Hydrochloride from a Viscous Solution when Mixed Together |
Vol. 10 No. 3 |
237 |
| Chemical Stability of Diclofenac Sodium Injection |
Vol. 10 No. 2 |
154 |
| Extended Stability of Oxytocin in Common Infusion Solutions |
Vol. 10 No. 2 |
156 |
| Stability of Morphine Sulfate in Polypropylene Infusion Bags for Use in Patient-Controlled Analgesia Pumps for Postoperative Pain Management |
Vol. 10 No. 1 |
69 |
| Stability of Phenytoin Sodium Suspensions for the Treatment of Open Wounds |
Vol. 10 No. 1 |
74 |
| Chemical Stability of Fentanyl in Polypropylene Syringes and Polyvinylchloride Bags |
Vol. 9 No. 6 |
482 |
| Chemical Stability of Perphenazine in Oral Liquid Dosage Forms |
Vol. 9 No. 6 |
484 |
| Stability and Subjective Taste Acceptability of Four Glycopyrrolate Solutions for Oral Administration |
Vol. 9 No. 5 |
396 |
| Chemical Stability of Hydralazine Hydrochloride after Reconstruction in 0.9% Sodium Chloride Injection or 5% Dextrose Injection for Infusion |
Vol. 9 No. 5 |
399 |
| Stability of Sotalol Hydrochloride in Extemporaneously Prepared Oral Suspension Formulations |
Vol. 9 No. 5 |
402 |
| Physical and Chemical Stability of Palonosetron Hydrochloride with Fluorouracil and with Gemcitabine Hydrochloride during Simulated Y-site Administration |
Vol. 9 No. 4 |
320 |
| Stability of Nebulizer Admixtures |
Vol. 9 No. 4 |
323 |
| Physical and Chemical Stability of Palonosetron Hydrochloride with Lorazepam and Midazolam Hydrochloride during Simulated Y-Site Administration |
Vol. 9 No. 3 |
235 |
| Physical and Chemical Stability of Palonosetron Hydrochloride with Topotecan Hydrochloride and Irinotecan Hydrochloride during Simulated Y-Site Administration |
Vol. 9 No. 3 |
238 |
| Chemical Stability of Isoniazid in an Oral Liquid Dosage Form |
Vol. 9 No. 2 |
165 |
| Chemical Stability of Metoclopramide Hydrochloride Injection Diluted with 0.9% Sodium Chloride Injection in Polypropylene Syringes at Room Temperature |
Vol. 9 No. 1 |
72 |
| Stability of an Extemporaneously Compounded Propylthiouracil Suspension |
Vol. 9 No. 1 |
82 |
| Stability of Extemporaneous Oral Ribavirin Liquid Preparation |
Vol. 8 No. 6 |
486 |
| Chemical Stability of Methadone Concentrate and Powder Diluted in Orange-Flavored Drink |
Vol. 8 No. 6 |
489 |
| Preparation and Characterization of a Compounded Aqueous Human Insulin Suspension |
Vol. 8 No. 6 |
492 |
| Book and Literature Reviews |
Vol. 8 No. 5 |
324 |
| Compatibility and Stability of Aloxi (Palonosetron Hydrochloride) Admixed With Dexamethasone Sodium Phosphate |
Vol. 8 No. 5 |
398 |
| Chemical Stability of Terbutaline Sulfate Injection After Diluting With Normal Saline When Stored at Room Temperature in Polyvinylchloride Bags |
Vol. 8 No. 5 |
404 |
| Physical and Chemical Stability of Trepostinil Sodium Injection Packaged in Plastic Syringe Pump Reservoirs. |
Vol. 8 No. 3 |
228 |
| Long-Term Stability of Trimix: A Three-Drug Injection Used to Treat Erectile Dysfunction. |
Vol. 8 No. 3 |
231 |
| Stability of Zidovudine and Ranitidine in 0.9% sodium Chloride and 5% Dextrose Injections Stored at Ambient Temperature (23 ± 2°C) and 4°C in 50-mL Polyvinylchloride Bags Up to 24 Hours. |
Vol. 8 No. 3 |
236 |
| Extemporaneous Formulation and Stability Testing of Mexiletine HCl Solution |
Vol. 8 No. 2 |
147 |
| Chemical Stability of Phenylephrine HCl After Reconstitution in 0.9% Sodium Chloride Injection for Infusion |
Vol. 8 No. 2 |
153 |
| Effect of Freezing, Long-Term Storage and Microwave Thawing on the Stability of Tramadol in 5% Dextrose Infusion in Polyvinyl Chloride Bags |
Vol. 8 No. 2 |
156 |
| Vancomycin HCl and Heparin Sodium Injection |
Vol. 8 No. 1 |
60 |
| Stability of Zidovudine and Dobutamine HCl Injections in 0.9% Sodium Chloride and 5% Dextrose Injections Stored at Ambient Temperature (23 ± 2°C) and 4°C in 50-mL Polyvinyl Chloride Bags Up to 24 Hours |
Vol. 8 No. 1 |
73 |
| Stability of Oral Liquid Dosage Forms of Glycopyrrolate Prepared with the Use of Powder |
Vol. 7 No. 5 |
386 |
| Formulation and Accelerated Stability Studies for an Extemporaneous Suspension of Amiodarone Hydrochloride |
Vol. 7 No. 5 |
389 |
| Formulation Development and Stability Testing of Extemporaneous Suspension Prepared From Dapsone Tablets |
Vol. 7 No. 3 |
233 |
| Stability of Clindamycin Phosphate in AutoDose Infusion System Bags |
Vol. 7 No. 2 |
149 |
| Chemical Stability of Cefazolin Sodium after Reconstituting in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 7 No. 2 |
152 |
| Quantification of Total Dexamethasone Phosphate Delivery by Iontophoresis |
Vol. 7 No. 2 |
155 |
| Stability of Glycopyrrolate Injection at Ambient Temperature and 4°C in Polypropylene Syringes |
Vol. 7 No. 1 |
65 |
| Stability of Succinylcholine Chloride Injection at Ambient Temperature and 4 Degree C in Polypropylene Syringes |
Vol. 7 No. 1 |
68 |
| Chemical Stability of Furosemide in Minibags and Polypropylene Syringes |
Vol. 6 No. 6 |
468 |
| Stability of Neostigmine Methylsulfate Injection at Ambient Temperature and 4°C in Polypropylene Syringes |
Vol. 6 No. 6 |
475 |
| pH Stability of Injectable Fentanyl, Bupivacaine, or Clonidine Solution or a Ternary Mixture in 0.9% Sodium Chloride in Two Types of Polypropylene Syringes |
Vol. 6 No. 6 |
471 |
| Stability of Lidocaine Hydrochloride Injection at Ambient Temperature and 4°C in Polypropylene Syringes |
Vol. 6 No. 5 |
388 |
| Effect of Freezing, Long-Term Storage, and Microwave Thawing on the Stability of Cefepime in 5% Dextrose Infusion Polyvinyl Chloride Bags |
Vol. 6 No. 5 |
391 |
| Chemical Stability of Dexamethasone Sodium Phosphate After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes |
Vol. 6 No. 5 |
395 |
| Stability of Tubocurarine Chloride Injection at Ambient Temperature and 4°C in Polypropylene Syringes |
Vol. 6 No. 4 |
308 |
| Compatibility Screening of Bivalirudin During Simulated Y-Site Administration with Other Drugs |
Vol. 6 No. 4 |
311 |
| Stability of Ketamine Hydrochloride Injection After Reconstitution in Water for Injection and Storage in 1-mL Tuberculin Polypropylene Syringes for Pediatric Use |
Vol. 6 No. 4 |
316 |
| pH and Osmolarity, A Review of |
Vol. 6 No. 3 |
216 |
| Stability of Ampicillin Sodium, Nafcillin Sodium, and Oxacillin Sodium in AutoDose Infusion System Bags |
Vol. 6 No. 3 |
226 |
| Compatibility Screening of Precedex During Simulated Y-Site Administration with Other Drugs |
Vol. 6 No. 3 |
230 |
| Stability of Cefotaxime Sodium After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 6 No. 3 |
234 |
| Stability of Gentamicin Sulfate and Tobramycin Sulfate in AutoDose Infusion System Bags |
Vol. 6 No. 2 |
152 |
| Stability of 4-Aminopyridine and 3,4-Diaminopyridine Oral Capsules |
Vol. 6 No. 2 |
155 |
| Physical and Chemical Stability of Morphine Sulfate 5-mg/mL and 50-mg/mL Packaged in Plastic Syringes |
Vol. 6 No. 1 |
62 |
| Physical and Chemical Stability of Low and High Concentrations of Morphine Sulfate with Clonidine Hydrochloride Packaged in Plastic Syringes |
Vol. 6 No. 1 |
66 |
| Physical and Chemical Stability of Low and High Concentrations of Morphine Sulfate with Bupivacaine Hydrochloride Packaged in Plastic Syringes |
Vol. 6 No. 1 |
70 |
| Physical and Chemical Stability of Hydromorphone Hydrochloride 1.5- and 80-mg/mL Packaged in Plastic Syringes |
Vol. 6 No. 1 |
74 |
| Tissue Plasminogen Activator (TPA) 0.5-mg/mL, 1.0-mg/mL, or 2.0-mg/mL for Catheter Occlusion |
Vol. 5 No. 6 |
456 |
| Stability of an Oral Liquid Dosage Form of Glycopyrrolate Prepared from Tablets |
Vol. 5 No. 6 |
480 |
| Stability of Pentobarbital Sodium After Reconstitution in 0.9% Sodium Chloride Injection and Repackaging in Glass and Polypropylene Syringes |
Vol. 5 No. 6 |
482 |
| Stability of Ephedrine Sulfate at Ambient Temperature and 4°C in Polypropylene Syringes |
Vol. 5 No. 5 |
394 |
| Assessment of the Stability of Teicoplanin in Intravenous Infusions |
Vol. 5 No. 5 |
397 |
| Analytical Testing Facilities and Products |
Vol. 5 No. 4 |
284 |
| Incompatibilities of Lansoprazole Injection with Other Drugs During Simulated Y-Site Coadministration |
Vol. 5 No. 4 |
314 |
| Compatibility and Stability of Potassium Chloride and Magnesium Sulfate in 0.9% Sodium Chloride Injection and 5% Dextrose Injection Solutions |
Vol. 5 No. 4 |
323 |
| Irrigation with Piperacillin for the Treatment of Bladder Infection: A Case Study |
Vol. 5 No. 3 |
195 |
| Stability of Piperacillin Sodium After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 5 No. 3 |
230 |
| Stability of Oral Liquid Dosage Forms of Ethacrynic Acid |
Vol. 5 No. 3 |
232 |
| Chemical Stability of Methylprednisolone Sodium Succinate After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes |
Vol. 5 No. 2 |
148 |
| Stability of Cefepime Hydrochloride After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 5 No. 2 |
151 |
| Stability and Dissolution of Lozenge and Emulsion Formulations of Metronidazole Benzoate |
Vol. 5 No. 2 |
153 |
| Stability Issues for Compounding Extemporaneously Prepared Oral Formulations for Pediatric Patients |
Vol. 5 No. 1 |
9 |
| Sterile-Product Preparations: Mix or Buy? |
Vol. 5 No. 1 |
59 |
| Compatibility Screening of Hextend During Simulated Y-Site Administration with Other Drugs |
Vol. 5 No. 1 |
69 |
| Stability of Ethacrynate Sodium After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 5 No. 1 |
73 |
| Stability of Acyclovir Sodium After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 5 No. 1 |
75 |
| Compatibility and Stability of Linezolid Injection Admixed with Gentamicin Sulfate and Tobramycin Sulfate |
Vol. 4 No .6 |
476 |
| Stability of Nafcillin Sodium After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 4 No .6 |
480 |
| Stability of Levothyroxine Sodium Injection in Polypropylene Syringes |
Vol. 4 No .6 |
482 |
| Stability of Hydrocortisone Sodium Succinate After Reconstitution in 0.9% Sodium Chloride Injection and Storage in Polypropylene Syringes for Pediatric Use |
Vol. 4 No. 5 |
396 |
| Stability of Lisinopril Syrup (2 mg/mL) Extemporaneously Compounded from Tablets |
Vol. 4 No. 5 |
398 |
| Short Communication: Compounding for Implantable Pumps |
Vol. 4 No. 4 |
280 |
| Dacarbazine 8-mg/mL, Doxorubicin HCl 0.8-mg/mL and Ondansetron 0.64-mg/mL injection |
Vol. 4 No. 4 |
296 |
| Doxorubicin HCl 0.4-mg/mL, Ondansetron HCl 0.48-mg/mL and Vincristine Sulfate 14-mcg/mL Injection |
Vol. 4 No. 4 |
298 |
| Microbiological Stability of a Fentanyl, Bupivacaine and Clonidine Mixture in a 0.9% Sodium Chloride Infusion Stored in Syringes and Reservoirs |
Vol. 4 No. 4 |
318 |
| Three Drug Stability Lives |
Vol. 4 No. 3 |
190 |
| Stability of Morphine-Ketamine Mixtures in 0.9% Sodium Chloride Injection Packaged in Syringes, Plastic Bags and MEDICATION CASSETTEª Reservoirs |
Vol. 4 No. 3 |
225 |
| Simple High-Performance Liquid Chromatographic Method for Simultaneous Determination of Fusidic Acid and Betamethasone Dipropionate in a Cream Formulation |
Vol. 4 No. 3 |
229 |
| Stability of an Oral Liquid Dosage Form of Trovafloxacin Mesylate and Its Quantitation in Tablets Using High-Performance Liquid Chromatography |
Vol. 4 No. 3 |
233 |
| Some Studies of the Stability of Compounded Cefazolin Ophthalmic Solution |
Vol. 4 No. 2 |
146 |
| Effect of Some Antioxidants on the Color Change of White Lotion |
Vol. 4 No. 2 |
154 |
| Stability of Ranitidine Hydrochloride with Cefazolin Sodium, Cefbuperazone Sodium, Cefoxitin Sodium and Cephalothin Sodium during Simulated Y-Site Administration |
Vol. 4 No. 2 |
150 |
| Compounding Intrathecal Medications |
Vol. 4 No. 1 |
24 |
| Particulates in Parenterals |
Vol. 4 No. 1 |
43 |
| Stability of Alatrofloxacin Mesylate in 5% Dextrose Injection and 0.45% Sodium-Chloride Injection |
Vol. 4 No. 1 |
66 |
| Naratriptan HCl in Extemporaneously Compounded Oral Suspensions |
Vol. 4 No. 1 |
69 |
| Physicochemical Stability of Compounded Creams Containing alpha-Hydroxy Acids |
Vol. 4 No. 1 |
72 |
| Operation of a Dry-Heat Sterilizing Oven and Validation of this Procedure |
Vol. 3 No. 6 |
488 |
| Stability of Dobutamine Hydrochloride 4 mg/mL in 5% Dextrose Injection at 5 and 23 degrees C |
Vol. 3 No. 5 |
412 |
| Physical Compatibility of Calcium Acetate and Potassium Phosphates in Parenteral Nutrition Solutions Containing Aminosyn II |
Vol. 3 No. 5 |
415 |
| Extemporaneous Formulations in Pediatric Patients |
Vol. 3 No. 4 |
274 |
| Parenteral Admixture with Y-Site Administration |
Vol. 3 No. 4 |
303 |
| Vancomycin and Ceftazidime in Peritoneal Dialysis Solution |
Vol. 3 No. 4 |
306 |
| Veterinary Flavor Suggestions |
Vol. 3 No. 3 |
186 |
| Fosphenytoin Y-site Stability Studies with Lorazepam and Midazolam Hydrochloride |
Vol. 3 No. 3 |
235 |
| Compatibility of Docetaxel with Selected Drugs during Simulated Y-Site Administration |
Vol. 3 No. 3 |
241 |
| Quantitation of Testosterone in Suspension using High Performance Liquid Chromatography |
Vol. 3 No. 3 |
239 |
| Analysis of Extemporaneous Alprostadil Formulations |
Vol. 3 No. 2 |
148 |
| Stability of Extemporaneously Prepared Sterile Testosterone Solution in 0.9% Sodium Chloride Solution Large-Volume Parenterals in Plastic Bags |
Vol. 3 No. 2 |
156 |
| Standard Operating Procedure for Performing Physical Quality Assessment of Suppositories, Troches, Lollipops and Sticks |
Vol. 3 No. 1 |
56 |
| Stability of Four Commercial Products Delivered by Mail Order |
Vol. 3 No. 1 |
59 |
| Y-Site Stability of Fosphenytoin and Sodium Phenobarbital |
Vol. 3 No. 1 |
64 |
| Five-Day Stability of Vinorelbine in 5% Dextrose Injection and in 0.9% Sodium Chloride Injection at Room Temperature |
Vol. 3 No. 1 |
67 |
| Chemical Stability of Meperidine Hydrochloride in Polypropylene Syringes |
Vol. 2 No. 6 |
463 |
| Stability of Sufentanil in a Syringe Pump Under Simulated Epidural Infusion |
Vol. 2 No. 6 |
466 |
| Stability of Albuterol in Continuous Nebulization |
Vol. 2 No. 5 |
394 |
| The Stability of Amphotericin B in a Mixture of Fungizone and Optimoist |
Vol. 2 No. 4 |
311 |
| Stability of Ciprofloxacin in Extemporaneous Oral Liquid Dosage Form |
Vol. 2 No. 4 |
314 |
| Compatibility and Stability of Ranitidine Hydrochloride with Six Cephalosporins During Simulated Y-Site Administration |
Vol. 2 No. 4 |
318 |
| Stability of Lorazepam in 5% Dextrose Injection |
Vol. 2 No. 4 |
322 |
| Paclitaxel Compatibility with IV Express Filter Unit |
Vol. 2 No. 3 |
243 |
| Stability of Milrinone Lactate in 5% Dextrose Injection and 0.9% Sodium Chloride Injection at Concentrations of 400, 600, 800 mcg/mL |
Vol. 2 No. 3 |
246 |
| Stability of Milrinone Lactate 200 mcg/mL in 5% Dextrose Injection and 0.9% Sodium Chloride Injection |
Vol. 2 No. 2 |
168 |
| Stability of Indomethacin in 0.9% Sodium Chloride Injection |
Vol. 2 No. 2 |
170 |
| The pH Value of Urea Solutions in Purified Water |
Vol. 2 No. 1 |
76 |
| Physical Compatibility and Chemical Stability of Atracurium Besylate and Midazolam Hydrochloride during Intravenous Coinfusion |
Vol. 2 No. 1 |
79 |
| Stability of Mechlorethamine Hydrochloride 0.01% Ointment in Aquaphor® Base |
Vol. 2 No. 1 |
89 |
| Basic Statistical Concepts for Evaluating Pharmaceutical Compounding Literature: Part 1.Statistics for Continuous Data and Stability Studies |
Vol. 1 No. 6 |
395 |
| Stability of Two Concentrations of Heparin Sodium Prefilled in CADD-Micro Pump Syringes |
Vol. 1 No. 6 |
433 |
| Stability of Cefepime Hydrochloride Dextrose in 5% Dextrose Injection and 0.9% Sodium Chloride Injection |
Vol. 1 No. 6 |
435 |
| Short-Term Stability of Atenolol in Oral Liquid Formulations |
Vol. 1 No. 6 |
437 |
| Stability of Clonazepam Suspension in HSC Vehicle |
Vol. 1 No. 6 |
440 |
| Drug Stability and Compatibility: Special Considerations for Home Health Care |
Vol. 1 No. 5 |
301 |
| Chemical Stability of Amiodarone Hydrochloride in Intravenous Fluids |
Vol. 1 No. 5 |
347 |
| Some Quality Control Tests on Chromium Picolinate in Solid Dosage Forms |
Vol. 1 No. 5 |
349 |
| The Stability of Lisinopril as an Extemporaneous Syrup |
Vol. 1 No. 5 |
352 |
| Compatibility of Vancomycin Hydrochloride and Famotidine in 5% Dextrose Injection |
Vol. 1 No. 5 |
354 |
| Compatibility of Warfarin Sodium with Selected Drugs and Large-Volume Parenteral Solutions |
Vol. 1 No. 5 |
356 |
| Stability of Ceftriaxone Sodium When Mixed with Metronidazole Injection |
Vol. 1 No. 4 |
280 |
| Stability of Mitomycin Aqueous Solution When Stored in Tuberculin Syringes |
Vol. 1 No. 4 |
282 |
| Parenteral Admixture Incompatibilities:An Introduction |
Vol. 1 No. 3 |
165 |
| Physical Stability of Urea Topical Formulations |
Vol. 1 No. 3 |
168 |
| The Formulation Development and Stability of Spironolactone Suspension |
Vol. 1 No. 3 |
195 |
| The Formulation Development and Stability of Metronidazole Suspension |
Vol. 1 No. 3 |
200 |
| Stability of Ketorolac Tromethamine in 5% Dextrose Injection and 0.9% Sodium Chloride Injections |
Vol. 1 No. 3 |
206 |
| Stability of Cefmetazole Sodium in 5% dextrose Injection and 0.9% Sodium Chloride Injection |
Vol. 1 No. 3 |
208 |
| Particle Size Distribution of Propofol Injection from Ampules and Vials: The Benefits of Filitration |
Vol. 1 No. 2 |
118 |
| The Compatibility of Common Respiratory Therapy Drug Combinations |
Vol. 1 No. 2 |
121 |
| Stability of Vancomycin HCl in MEDICATION CASSETTE Reservoirs |
Vol. 1 No. 2 |
123 |
| Quantitation of Metoprolol Tartrate and Propranolol Hydrochloride in Pharmaceutical Dosage Forms: Stability of Metoprolol in an Aqueous Mixture |
Vol. 1 No. 2 |
125 |
| Stability of Allopurinol Suspension Compounded from Tablets |
Vol. 1 No. 2 |
128 |
| Stability of Aminocaproic Acid Injection Admixtures in 5% Dextrose Injection and 0.9% Sodium Chloride Injection |
Vol. 1 No. 2 |
132 |
| Compounding an Extended Stability Admixture of Paclitaxel for Long-Term Infusion |
Vol. 1 No. 1 |
49 |