Prescription medication · Progestin-Only Oral Contraceptive

norethindrone

Also sold as Camila, Errin. These pills are used to prevent pregnancy.

Data updated 2026-05-15

5,342
FDA reportsLightly reported
10
InteractionsSeveral interactions
$0.08
Generic price (NADAC)

What the data shows

norethindrone (Camila) is a prescription Progestin-Only Oral Contraceptive, reported less often than most tracked drugs (5,342 FDA reports), with 10 documented drug interactions.

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.

norethindrone (Camila) is a prescription Progestin-Only Oral Contraceptive. These pills are used to prevent pregnancy.

Camila and Errin are progestin-only birth control pills. They help prevent pregnancy.

Drug Pricing (NADAC)

Generic Price

$0.08/unit

Generic Available

Yes (86 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

These pills are used to prevent pregnancy.

Common side effects

Nausea, Vomiting, Gastrointestinal symptoms (like cramps and bloating)

Key warnings

Cigarette smoking increases your risk of serious heart problems from birth control pills.

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

How It Works

Camila and Errin contain a progestin hormone. This hormone prevents pregnancy by stopping ovulation (the release of an egg from the ovary). It also thickens cervical mucus, making it harder for sperm to reach the egg.

Side Effects (from patient reports)

Based on 5,342 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for norethindrone, 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 norethindrone each year to the FDA Adverse Event Reporting System (FAERS).

0200400600 20042007201020132016201920222025 426

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

Where norethindrone sits

norethindrone has more FDA adverse-event reports than 26% 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 norethindrone; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 5,342 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

5,342

Reports Mentioning Death

80

1.5% of reports — not proof of cause

Hospitalization Reports

945

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 4,688 (99%)
Male 40 (1%)

Age Distribution

0–17 261
18–44 2,242
45–64 697
65–74 51
75+ 10

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 NAUSEA 449
2 HEADACHE 424
3 HOT FLUSH 370
4 FATIGUE 322
6 PAIN 308
8 VAGINAL HAEMORRHAGE 278
9 ABDOMINAL PAIN 268
10 ARTHRALGIA 228
11 DIARRHOEA 224
12 DIZZINESS 221
13 ANXIETY 204
14 MIGRAINE 202
15 DEPRESSION 199
16 VOMITING 199
17 PELVIC PAIN 181

Reactions in Death Reports

DEATH 22
PNEUMONIA 11
RESPIRATORY FAILURE 10
CARDIAC ARREST 7
DYSPNOEA 6
GENERAL PHYSICAL HEALTH DETERIORATION 5
HYPERTENSION 5
PAIN 5
RENAL FAILURE 5
ACUTE KIDNEY INJURY 4

Reactions in Hospitalization Reports

HEADACHE 85
NAUSEA 82
PAIN 77
DYSPNOEA 76
VOMITING 68
ABDOMINAL PAIN 63
FATIGUE 61
DIARRHOEA 55
PYREXIA 55
PULMONARY EMBOLISM 50

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

Serious Warnings

Cigarette smoking increases your risk of serious heart problems from birth control pills. This risk is higher if you are over 35 and smoke. You should not take this medication if you are over 35 and smoke.

Known Drug Interactions

John's Wort (CYP450 inducer; P-gp inducer) Significantly Reduced Contraindicated Oral Contraceptives containing ethinyl estradiol and norethindrone (CYP2C19 Inhibition) Increased Monitoring for adverse reactions and toxicity related to voriconazole is recommended when coadministered with oral contraceptives. Oral Contraceptives containing ethinyl estradiol and norethindrone (CYP3A4 Inhibition) Increased Monitoring for adverse reactions related to oral contraceptives is recommended during coadministration.

Mechanism: Voriconazole slows down the process your body uses to get rid of the birth control pill. This can lead to higher levels of the birth control in your blood and increase your risk of side effects.

Oral Contraceptives: May increase plasma levels of norethindrone and ethinyl estradiol; consider this effect when selecting an oral contraceptive (7.3 ). Table 4: Atorvastatin Effects on Other Drugs Oral Contraceptives Clinical Impact: Co-administration of atorvastatin and an oral contraceptive increased plasma concentrations of norethindrone and ethinyl estradiol [see Clinical Pharmacology (12.3) ].

Mechanism: Taking atorvastatin can raise the levels of this hormone in your bloodstream.

Drug Interactions: Pharmacokinetic Parameters for Colchicine Tablets in the Presence of the Coadministered Drug Coadministered Drug Dose of Coadministered Drug (mg) Dose of Colchicine Tablets (mg) N % Change in Colchicine Concentrations from Baseline (Range: Min – Max) C max AUC 0-t Cyclosporine 100 mg single dose 0.6 mg single dose 23 270.0 (62.0 to 606.9) 259.0 (75.8 to 511.9) Clarithromycin 250 mg twice daily, 7 days 0.6 mg single dose 23 227.2 (65.7 to 591.1) 281.5 (88.7 to 851.6) Ketoconazole 200 mg twice daily, 5 days 0.6 mg single dose 24 101.7 (19.6 to 219.0) 212.2 (76.7 to 419.6)...

Mechanism: There is no known significant interaction between these two medications. They do not interfere with how each other is processed by the body.

7 DRUG INTERACTIONS Concomitant use with colesevelam hydrochloride may decrease the exposure of the following drugs: Drugs with a narrow therapeutic index (e.g., cyclosporine), phenytoin, thyroid hormone replacement therapy, warfarin, oral contraceptives containing ethinyl estradiol and norethindrone, olmesartan medoxomil, and sulfonylureas (glimepiride, glipizide, glyburide). Oral Contraceptives Containing Ethinyl Estradiol and Norethindrone Clinical Impact: In vivo drug interactions studies showed a decrease in exposure of ethinyl estradiol and norethindrone when coadministered with...

Mechanism: Colesevelam can reduce the amount of birth control medicine that enters your body. This happens because the drug can trap the birth control in your digestive system before it can work.

ethinyl estradiol, norethindrone, drospirenone ↓ ethinyl estradiol ↓ norethindrone drospirenone: effects unknown For co-administration with drospirenone, clinical monitoring is recommended due to the potential for hyperkalemia.

Mechanism: Darunavir can lower the amount of birth control hormones in your body, which might make the medication less effective.

Check all your medications →

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

Common Questions

What if I experience breakthrough bleeding?
Breakthrough bleeding or spotting is common, especially during the first few months. If it continues, talk to your doctor.
Can this pill cause weight gain?
Some women experience weight changes, either gain or loss, while taking this pill.
Will this pill protect me from STIs?
No, this pill does not protect against sexually transmitted infections (STIs). Use condoms to protect yourself from STIs.
What should I do if I vomit after taking the pill?
If you vomit within 3-4 hours of taking the pill, it may not be fully absorbed. Take another pill as soon as possible and use a backup method of birth control for the next 7 days.
Can I still get pregnant if I take this pill?
This pill is very effective if taken correctly. However, no birth control method is 100% effective.
Will this pill affect my mood?
Some women experience mood changes, including depression, while taking this pill. Talk to your doctor if you have concerns.
Can I take this pill if I have high blood pressure?
Talk to your doctor before taking this pill if you have high blood pressure.
Does this pill have any effect on my cholesterol?
This pill can affect your cholesterol levels. Your doctor may monitor your cholesterol while you are taking this pill.
Can I take this pill if I have a history of blood clots?
You should not take this pill if you have a history of blood clots.
What if I want to stop taking this pill?
You can stop taking this pill at any time. Talk to your doctor about other birth control options if you do not want to get pregnant.
What are the common side effects of norethindrone?
The registry lists Nausea, Vomiting, Gastrointestinal symptoms (like cramps and bloating), Breakthrough bleeding or spotting, Changes in menstrual flow among the most-reported FAERS reaction terms for norethindrone. The compiled record contains 5,342 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does norethindrone interact with other medications?
The registry has 10 documented interaction rows for norethindrone. Notable source-record pairings include voriconazole, atorvastatin, colchicine. These rows are not a complete medication review.
What drug class is norethindrone?
norethindrone belongs to the Progestin-Only Oral Contraceptive drug class. It requires a prescription (Rx). These pills are used to prevent pregnancy.
What pregnancy or breastfeeding source fields are listed for norethindrone?
The FDA label for norethindrone contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

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

Compare norethindrone vs abiraterone side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for norethindrone: 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.

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What the FDA Data Shows for norethindrone

The FDA label for norethindrone (sold under brand names such as Camila, Errin) classifies it as a prescription-only medication in the Progestin-Only Oral Contraceptive class. These pills are used to prevent pregnancy. Official labeling lists 9 commonly reported side effects, including Nausea, Vomiting, Gastrointestinal symptoms (like cramps and bloating).

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 5,342 voluntary reports. The database also lists 10 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. NADAC pricing from CMS shows a generic unit cost of $0.08.

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: January 29, 2026

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