Crofab Powder For Solution For Injection 1G Drug Medication Dosage Information
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CroFab: Powder for solution for injection (1g)

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What is this Medicine?

CROTALIDAE POLYVALALENT IMMUNE FAB is an anti-venom. It is used to treat patients who have been bitten by certain poisonous snakes, like rattlesnakes and water moccasins.

In-Depth Information
Select a Medication

CroFab 1g Powder for Injection

NDC: 506330110
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Crotalid Snake Bite

Storage Information
Do not freeze
Reconstituted product must be used within 4 hours
Store between 36 to 46 degrees F
CroFab 1g Powder for Injection

Reported Side Effects for CroFab 1g Powder for Injection

Upset Stomach Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
Wheezing Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: RAPID
Rapid Breathing Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: EARLY
Rapid Heart Rate Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: RAPID
Skin Redness Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: EARLY
Lightheadedness Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
Chills Incidence:
1.0-10.0%*
Severity: MILD
Onset: RAPID
Chest Pain Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: EARLY
Breathing Difficulties Incidence:
1.0-10.0%*
Severity: SEVERE
Onset: RAPID
Back Pain Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Anaphylactoid Reactions Incidence:
1.0-10.0%*
Severity: SEVERE
Onset: RAPID
Serum Sickness Incidence:
1.0-10.0%*
Severity: SEVERE
Onset: DELAYED
Itching Incidence:
1.0-10.0%*
Severity: MILD
Onset: RAPID
Muscle Pain Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
Low Blood Pressure Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: RAPID
Excessive Sweating Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Headache Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
Fever Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
Swelling Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: DELAYED
Shortness Of Breath Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: EARLY
Cough Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Nervousness Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Decreased Appetite Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Angioedema Incidence:
1.0-10.0%*
Severity: SEVERE
Onset: RAPID
Hives Incidence:
>10.0%*
Severity: MILD
Onset: RAPID
Skin Rash Incidence:
>10.0%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


Learning More About
Visit the Drug Summary page where you can:
  • Get answers to Frequently Asked Questions (FAQs)
  • Find other class related drugs
  • Find additional patient usage statistics
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