Prescription medication · Parathyroid Hormone Analog

teriparatide

Also sold as Forteo. This medicine treats osteoporosis in women after menopause who have a high chance of breaking a bone.

Data updated 2026-05-15

111,257
FDA reportsOften reported
1
InteractionFew interactions
52% less
Generic vs brandBig savings
$1726.47
Brand price (NADAC)

What the data shows

teriparatide (Forteo) is a prescription Parathyroid Hormone Analog, more reported than most tracked drugs (111,257 FDA reports), whose generic runs roughly half the brand price or less (52% less).

Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.

teriparatide (Forteo) is a prescription Parathyroid Hormone Analog. This medicine treats osteoporosis in women after menopause who have a high chance of breaking a bone.

Teriparatide (Forteo) is a medicine that helps to strengthen your bones. It is similar to a natural hormone in your body that helps build bone.

Drug Pricing (NADAC)

Brand Price

$1726.47/unit

Generic Price

$832.72/unit

Generic Savings

52%

Generic Available

Yes (3 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

Compare with Another Drug → Full Side Effects Report →

What it does

This medicine treats osteoporosis in women after menopause who have a high chance of breaking a bone.

Common side effects

Joint pain, General pain, Feeling sick to your stomach (nausea)

Key warnings

This medicine may increase your risk of a type of bone cancer called osteosarcoma.

The sections below are summarized in plain English from teriparatide's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

Teriparatide works like a hormone called parathyroid hormone. This hormone helps your body build new bone. By building new bone, this medicine helps make your bones stronger and less likely to break.

Side Effects (from patient reports)

Based on 111,257 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for teriparatide, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for teriparatide each year to the FDA Adverse Event Reporting System (FAERS).

010,00020,00030,00040,00050,000 20042007201020132016201920222025 2,061

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where teriparatide sits

teriparatide has more FDA adverse-event reports than 87% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is teriparatide; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 111,257 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

111,257

Reports Mentioning Death

5,261

4.7% of reports — not proof of cause

Hospitalization Reports

23,997

Top Indication

Osteoporosis

Gender Distribution

Female 99,360 (91%)
Male 10,239 (9%)

Age Distribution

0–17 63
18–44 1,153
45–64 15,718
65–74 18,058
75+ 25,089

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 NAUSEA 8,956
2 ARTHRALGIA 8,658
3 PAIN IN EXTREMITY 8,338
4 DIZZINESS 8,265
5 FALL 7,872
6 PAIN 7,516
7 FATIGUE 7,159
8 BACK PAIN 5,903
9 MUSCLE SPASMS 5,730
10 MALAISE 5,658
11 HEADACHE 5,461
12 ASTHENIA 5,426
13 INJECTION SITE ERYTHEMA 5,042
14 INJECTION SITE PAIN 4,807
15 INJECTION SITE BRUISING 4,762

Reactions in Death Reports

DEATH 2,901
PNEUMONIA 401
FALL 263
MYOCARDIAL INFARCTION 192
DYSPNOEA 162
CEREBROVASCULAR ACCIDENT 161
RENAL FAILURE 160
RESPIRATORY FAILURE 155
CARDIAC ARREST 149
ASTHENIA 139

Reactions in Hospitalization Reports

FALL 3,935
PNEUMONIA 1,575
HOSPITALISATION 1,503
ASTHENIA 1,397
PAIN 1,383
MALAISE 1,349
BACK PAIN 1,318
NAUSEA 1,299
DIZZINESS 1,192
PAIN IN EXTREMITY 1,127

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

Serious Warnings

This medicine may increase your risk of a type of bone cancer called osteosarcoma. You should not use this medicine if you have certain bone conditions, such as Paget's disease, bone cancer, or have had radiation to your bones. If you have high calcium levels in your blood, talk to your doctor before taking this medicine.

Known Drug Interactions

minor digoxin

Parathyroid Hormone Analog Teriparatide Sporadic case reports have suggested that hypercalcemia may predispose patients to digitalis toxicity. Teriparatide transiently increases serum calcium.

Mechanism: Teriparatide raises calcium levels in your blood, which can make the heart more sensitive to digoxin and lead to toxic effects.

This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

How long can I use teriparatide?
You should only use teriparatide for up to 2 years during your lifetime, unless your doctor says you still have a high risk of breaking a bone.
What should I do if the solution looks cloudy?
Do not use the medicine if the solution has solid particles or is cloudy or colored. It should be clear and colorless.
Can I inject this medicine into my muscle?
No, this medicine is only for injection under the skin (subcutaneous).
What if I have kidney stones?
Tell your doctor if you have kidney stones, as this medicine could make them worse.
Can this medicine affect my heart?
This medicine can cause a temporary drop in blood pressure when you first start taking it. Be careful when standing up.
What if I am taking digoxin?
Tell your doctor if you are taking digoxin, a heart medicine, as this medicine can affect how digoxin works.
Can children use this medicine?
No, this medicine is not approved for use in children.
What do I do if the pen seems to be malfunctioning?
Each pen contains extra volume to allow troubleshooting of the device 2 times.
Does this medicine cause allergic reactions?
In rare cases, some people have had severe allergic reactions to teriparatide. Seek immediate medical attention if you experience swelling or difficulty breathing.
What if I recognize I am pregnant while using this medicine?
Consider discontinuing teriparatide injection when pregnancy is recognized.
What are the common side effects of teriparatide?
The registry lists Joint pain, General pain, Feeling sick to your stomach (nausea) among the most-reported FAERS reaction terms for teriparatide. The compiled record contains 111,257 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does teriparatide interact with other medications?
The registry has 1 documented interaction rows for teriparatide. Notable source-record pairings include digoxin. These rows are not a complete medication review.
What drug class is teriparatide?
teriparatide belongs to the Parathyroid Hormone Analog drug class. It requires a prescription (Rx). This medicine treats osteoporosis in women after menopause who have a high chance of breaking a bone.
Is there a generic version of teriparatide?
Yes, generic teriparatide is available from 3 manufacturers. The generic costs $832.72 per unit compared to $1726.47 for the brand version, saving approximately 52%. Pricing is based on NADAC (National Average Drug Acquisition Cost) data from CMS.
What pregnancy or breastfeeding source fields are listed for teriparatide?
The FDA label for teriparatide contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

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

Compare teriparatide vs abaloparatide side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for teriparatide: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

Medication Guides

Save on teriparatide

Compare prices and find discounts at pharmacies near you. Free coupons can save up to 80% on prescriptions.

Disclosure: This link may earn us a commission at no extra cost to you. See our terms.

What the FDA Data Shows for teriparatide

The FDA label for teriparatide (sold under brand names such as Forteo) classifies it as a prescription-only medication in the Parathyroid Hormone Analog class. This medicine treats osteoporosis in women after menopause who have a high chance of breaking a bone. Official labeling lists 3 commonly reported side effects, including Joint pain, General pain, Feeling sick to your stomach (nausea).

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 111,257 voluntary reports. The database also lists 1 documented drug interaction derived from FDA labeling, with the top-flagged interaction rated minor severity. NADAC pricing from CMS shows a generic unit cost of $832.72 versus $1726.47 for the brand - a 52% generic savings.

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, and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.

Last updated: May 27, 2025

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page