You do not have permission to edit this page, for the following reason:

The action you have requested is limited to users in the group: Users.

Warning: This page already exists, but it does not use this form.

Instructions[edit | edit source]

Please read the tutorial here.

Please enter your author tag here:

Overview Statement[edit | edit source]

Is this an over-the-counter medicine? Step 1: Check the FDA label. Step 2: Select "Yes" from the drop-down menu if it is an over-the-counter medicine.
Please enter the generic name here:
Please indicate the class to which the drug belongs: Step 1: Search with the generic name at Drug Information Portal Step 2: Match the collected categories with FDA Established Pharmacologic Classes
Please describe which indications the FDA has approved the use of the drug: Step 1: Check the "Indications and Usage" section from the FDA label Step 2: Enter the FDA approved indications Step 3: Fit the context: (Drug name) is (a/an) (category a, category b, and category c) that is FDA approved for the treatment/prophylaxis/diagnosis/procedure of (indication a, indication b, and indication c). Step 4: Create hyperlinks for indications
Is there a Black Box warning associated with the drug? Step 1: Check the "Warnings" section from the FDA label Step 2: Select "Yes" from the drop-down menu if there is a Black Box Warning
Please list the common adverse reactions associated with the drug: Step 1: Collect adverse reactions from the "Highlights of Prescribing Information" section *Step 2: Fit the context: Common adverse reactions include (reaction a, reaction b, and reaction c).* Step 3: Create hyperlinks for adverse reactions

Black Box Warning[edit | edit source]

Please enter the title of the Black Box warning:
Please enter the body of the Black Box warning: <span style="clear;"></span>

Adult Indications and Dosage[edit | edit source]

Please enter FDA-labeled indications and dosing information for adults: Step 1: Check the "Dosage And Administration" section from the FDA label Step 2: Insert the dosing information for each indication
Please enter established off-label use and dosage for adults:
Please enter guideline-supported off-label use in this field:
Please enter non–guideline-supported off-label use in this field:

Pediatric Indications and Dosage[edit | edit source]

Please enter FDA-labeled indications and dosage information for children: Step 1: Check the "Dosage And Administration" section from the FDA label Step 2: Insert the dosing information for each indication
Please enter established off-label use and dosage for children:
Please enter guideline-supported off-label use in this field:
Please enter non–guideline-supported off-label use in this field:

Contraindications[edit | edit source]

Please enter the FDA reported contraindications:

Step 1: Check the "Contraindications" section from the FDA label

Step 2: Arrange the content into bullet points

Warnings[edit | edit source]

Please enter the FDA reported warnings associated with the drug:

Step 1: Check the "Warnings" section from the FDA label

Step 2: Arrange the content into bullet points

Adverse Reactions[edit | edit source]

Please enter the adverse reactions reported from clinical trial experience: Step 1: Check the "Adverse Reactions" section from the FDA label Step 2: Arrange the content based on organ systems
Please enter the adverse reactions reported from postmarketing experience: Step 1: Check the "Adverse Reactions" section from the FDA label Step 2: Arrange the content based on organ systems

Drug Interactions[edit | edit source]

Please enter established drug interactions:

Step 1: Check the "Drug Interactions" section from the FDA label

Step 2: Arrange the content into bullet points

Use in Specific Populations[edit | edit source]

FDA Pregnancy Category:
Please enter information related to the FDA pregnancy category:
Australian Pregnancy Category:
Please enter information related to the Australian pregnancy category:
Please enter information related to the use of the drug during labor and delivery:
Please enter information related to the use of the drug during nursing:
Please enter information related to the use of the drug in pediatrics:
Please enter information related to the use of the drug in geriatrics:
Please enter information related to the use of the drug and gender:
Please enter information related to the use of the drug and race:
Please enter information related to the use of the drug in patients with renal impairment:
Please enter information related to the use of the drug in patients with hepatic impairment:
Please enter information related to the use of the drug in females of reproductive potential and males:
Please enter information related to the use of the drug in immunocompromised patients:
Please enter information related to the use of the drug in condition of Others:	Title of Others section:
	Body of Others section:

Administration and Monitoring[edit | edit source]

Please enter information pertaining to drug administration here:
Please enter information pertaining to the drug monitoring here:

IV Compatibility[edit | edit source]

Please enter information pertaining to the IV compatibility here:

Overdose[edit | edit source]

Please enter information pertaining to the drug overdose here:

Pharmacology[edit | edit source]

Please enter the DrugBox2 template here: Step 1: Construct the Drugbox2 template based on the original drugbox template Step 2: Cultivate the structure image from PubChem Step 3: Rename and upload the image to accommodate the Drugbox2 template
Please enter information related to the mechanism of action:
Please enter information related to the structure:
Please enter information related to the pharmacodynamics:
Please enter information related to the pharmacokinetics:
Please enter information related to the nonclinical toxicology:

Clinical Studies[edit | edit source]

Please enter information pertaining to the clinical studies of the drug:

How Supplied[edit | edit source]

Please enter information pertaining to how the drug is supplied:
Please enter information pertaining to how the drug should be stored:

Package and Label Display Panel[edit | edit source]

Please enter the Package and Label Display Panel here:

[[File:XXXXX.png|thumb|none|400px|This image is provided by the National Library of Medicine.]]

Patient Counseling Information[edit | edit source]

Please enter the Patient Counseling Information here:

Precautions with Alcohol[edit | edit source]

Please describe any guideline on the concurrent use of the drug with alcohol:

Brand Names[edit | edit source]

Please enter the brand names here:

Look-Alike Drug Names[edit | edit source]

Please enter look-alike names that could be confused with the drug:

Price[edit | edit source]

Please enter the drugs a patient may want to compare for price:

Add Images[edit | edit source]

Add Another Image

Cancel

Edit DrugProjectForm: Chloramphenicol sodium succinate

Contents