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ergocalciferol

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Brand names: Drisdol, Calciferol

Vitamin D2 Supplement OTC

Ergocalciferol is a vitamin D2 supplement. It helps your body absorb calcium and phosphorus, which are important for strong bones.

What it does

This medicine treats conditions caused by low vitamin D levels.

Common side effects

No common side effects listed.

Key warnings

The range between helpful and harmful doses is very small.

How It Works

Ergocalciferol is a synthetic form of vitamin D2. It helps your body absorb calcium from the stomach and intestines. It also helps regulate calcium levels in your blood.

How to Take It

Take this medicine exactly as your doctor tells you. The dose will be based on your specific condition. You may need regular blood tests and X-rays while taking this medicine to monitor your progress. Make sure you get enough calcium in your diet.

Pregnancy & Breastfeeding

Tell your doctor if you are pregnant or breastfeeding. High doses of vitamin D during pregnancy can harm the baby. Talk to your doctor about the risks and benefits.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule.

Storage

Store at room temperature (77°F), away from light and moisture.

Side Effects (from patient reports)

Based on 240,932 FDA adverse event reports.

Tiredness
36,313
Feeling sick to your stomach
27,028
Loose stools
25,823
Head pain
24,765
Medicine not working
24,587
Pain
23,210
Using medicine for unapproved purpose
21,938
Difficulty breathing
19,348
Joint pain
19,250
Feeling lightheaded
18,670

FDA Adverse Event Report Analysis

Detailed analysis of 366,491 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 1999–2025.

Total Reports

366,491

Death-Related Reports

21,613

Hospitalization Reports

98,409

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 246,146 (71%)
Male 101,058 (29%)

Age Distribution

0–17 7,342
18–44 36,721
45–64 85,432
65–74 58,630
75+ 48,346

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 FATIGUE 36,312
2 NAUSEA 27,026
3 DIARRHOEA 25,824
4 HEADACHE 24,768
5 DRUG INEFFECTIVE 24,587
6 PAIN 23,207
7 OFF LABEL USE 21,938
8 DYSPNOEA 19,350
9 ARTHRALGIA 19,251
10 DIZZINESS 18,673
11 ASTHENIA 16,525
12 FALL 16,406
13 VOMITING 15,063
14 PAIN IN EXTREMITY 14,394
15 MALAISE 14,135

Reactions in Death Reports

DEATH 9,908
PNEUMONIA 2,194
OFF LABEL USE 2,169
FATIGUE 2,085
DYSPNOEA 2,037
DIARRHOEA 1,875
NAUSEA 1,735
PAIN 1,709
GENERAL PHYSICAL HEALTH DETERIORATION 1,682
ASTHENIA 1,664

Reactions in Hospitalization Reports

FATIGUE 9,636
PNEUMONIA 9,114
DYSPNOEA 8,929
FALL 8,586
NAUSEA 8,522
DIARRHOEA 8,216
PAIN 7,440
ASTHENIA 7,103
HEADACHE 6,581
VOMITING 6,516

Source: FDA FAERS (Adverse Event Reporting System) FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

The range between helpful and harmful doses is very small. Your doctor needs to closely supervise your dosage. Too much vitamin D can cause serious side effects, including kidney problems and tissue damage.

Common Questions

What is the strength of each capsule?
Each capsule contains 1,250 mcg (50,000 USP units) of vitamin D2.
How often will I need blood tests?
Your doctor will likely order blood tests every 2 weeks, or more often if needed.
Can I take this with other medications?
Tell your doctor about all the medicines you take, including mineral oil and thiazide diuretics.
What should I do if I experience side effects?
Contact your doctor if you experience any unusual symptoms.
How will I know if the medicine is working?
Your doctor will monitor your condition with blood tests and X-rays.
Can I drink alcohol while taking this medicine?
Ask your doctor or pharmacist if it is safe to drink alcohol while taking this medicine.
What happens if I take too much?
Taking too much vitamin D can be dangerous. Contact your doctor or seek medical attention immediately.
Is there a generic version of this medicine?
Yes, ergocalciferol is the generic name.
How long will I need to take this medicine?
Your doctor will determine how long you need to take this medicine based on your condition.
What should I avoid while taking this medicine?
Follow your doctor's instructions about diet and other medications.
What drug class is ergocalciferol?
ergocalciferol belongs to the Vitamin D2 Supplement drug class. It is available over the counter (OTC). This medicine treats conditions caused by low vitamin D levels.
Is ergocalciferol safe during pregnancy?
Tell your doctor if you are pregnant or breastfeeding. High doses of vitamin D during pregnancy can harm the baby. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.
Has ergocalciferol been recalled?
There is 1 recall associated with ergocalciferol products. Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes. Check the recalls section below for full details and affected products.

Active Recalls

Class II February 17, 2025

Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.

Safecor Health, LLC

Related Medications in Vitamin D2 Supplement

Other drugs grouped near ergocalciferol — same-class peers and common alternatives.

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Medication Guides

Related Health & Safety Data

What the FDA Data Shows for ergocalciferol

The FDA label for ergocalciferol (sold under brand names such as Drisdol, Calciferol) classifies it as an over-the-counter product in the Vitamin D2 Supplement class. This medicine treats conditions caused by low vitamin D levels. Labeling covers dosing, contraindications, and monitoring requirements derived from clinical trials.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 240,932 voluntary reports. Interaction data is drawn directly from FDA-approved prescribing information. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.

Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history (currently 1 recall record on file), and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: January 31, 2025

All federal data sources used on this page