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Norethindrone adverse events reported to FDA.

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Summary

FDA Adverse Reports: 7. View All

Norethindrone FDA safety alerts: 2003

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Norethindrone, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Norethindrone users, Learn more about unwanted side effects & find ways to reduce them. Browse Norethindrone Adverse Reports reported to FDA and participate in Norethindrone discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Norethindrone. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Norethindrone Adverse Effect Reports (FDA)

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6991742-2 | Malaise
on Sep 16, 2010 Female patient from UNITED STATES , 18 years of age, weighting 119.2 lb, was diagnosed with contraception and was treated with Norethindrone (View Usage). Patient experienced the following unwanted or unexpected effects: malaise. Norethindrone dosage: .

6978286-9 | Cholestasis Of Pregnancy, Epilepsy, Live Birth, Pregnancy On Oral Contraceptive, Premature Labour
Patient was taking Norethindrone (View Usage). Patient had the following side effects: cholestasis of pregnancy, epilepsy (What is epilepsy?), live birth, pregnancy on oral contraceptive, premature labour on Sep 03, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 35 years of age, weighting 119.0 lb, was diagnosed with epilepsy (What is epilepsy?) and. Norethindrone dosage: . During the same period patient was treated with MICONAZOLE (View Miconazole Review and Miconazole Label ), ARIPIPRAZOLE (View Aripiprazole Review and Aripiprazole Label ), DIHYDROCODEINE BITARTRATE INJ (View Dihydrocodeine Bitartrate Inj Review and Dihydrocodeine Bitartrate Inj Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ), SERTRALINE HYDROCHLORIDE (View Sertraline Hydrochloride Review and Sertraline Hydrochloride Label ). Patient was hospitalized.

6978285-7 | Atrial Septal Defect, Premature Baby, Ventricular Septal Defect
Adverse event was reported on Sep 03, 2010 by a Male patient taking Norethindrone (View Usage) (Dosage: ) . Location: UNITED KINGDOM , weighting 6.17 lb, After Norethindrone was administered, patient had the following side effects: atrial septal defect, premature baby, ventricular septal defect. During the same period patient was treated with MICONAZOLE (View Miconazole Review and Miconazole Label ), ARIPIPRAZOLE (View Aripiprazole Review and Aripiprazole Label ), DIHYDROCODEINE BITARTRATE INJ (View Dihydrocodeine Bitartrate Inj Review and Dihydrocodeine Bitartrate Inj Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ), SERTRALINE HYDROCHLORIDE (View Sertraline Hydrochloride Review and Sertraline Hydrochloride Label ).

6871340-1 | Spina Bifida
on Jul 13, 2010 Male patient from CANADA , weighting 6.42 lb, was treated with Norethindrone (View Usage). Patient experienced the following unwanted or unexpected effects: spina bifida (What is spina bifida?). Norethindrone dosage: .


6871339-5 | Abortion Incomplete, Pregnancy On Oral Contraceptive
on Jul 13, 2010 Female patient from CANADA , 23 years of age, was diagnosed with contraception and was treated with Norethindrone (View Usage). Patient had the following side effects: abortion incomplete, pregnancy on oral contraceptive. Norethindrone dosage: .

6822104-6 | Hepatic Enzyme Increased, Hepatitis Acute
Patient was taking Norethindrone (View Usage). After Norethindrone was administered, patient had the following side effects: hepatic enzyme increased, hepatitis acute on Jun 29, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 31 years of age, was diagnosed with contraception and. Norethindrone dosage: . During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), KALETRA (View Kaletra Review and Kaletra Label ), KIVEXA (View Kivexa Review and Kivexa Label ).

6168986-5 | Alopecia, Amnesia, Blood Pressure Increased, Burning Sensation, Chloasma, Confusional State, Hypoaesthesia, Oedema Peripheral
Adverse event was reported on Apr 24, 2009 by a Female patient taking Norethindrone (View Usage) (Dosage: 10mg Daily Po) was diagnosed with vaginal haemorrhage and. Location: UNITED STATES , 44 years of age, weighting 180.0 lb, Patient experienced the following unwanted or unexpected effects: alopecia, amnesia, blood pressure increased, burning sensation, chloasma, confusional state, hypoaesthesia, oedema peripheral.


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Norethindrone Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

Jen   Kentucky 

10:40am on Monday, November 29th, 2010

Have been taking Micronr for 2 mnths. Have had heavy bleeding 6 of the 8 wks I have been on it. the ... read more »

To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Norethindrone risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Norethindrone quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Norethindrone use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Norethindrone Reactions
Abortion Incomplete
Alopecia
Amnesia
Atrial Septal Defect
Blood Pressure Increased
Burning Sensation
Chloasma
Cholestasis Of Pregnancy
Confusional State
EpilepsyWhat is Epilepsy?
Hepatic Enzyme Increased
Hepatitis Acute
Hypoaesthesia
Live Birth
Malaise
Oedema Peripheral
Pregnancy On Oral Contraceptive
Premature Baby
Premature Labour
Spina BifidaWhat is Spina bifida?
Ventricular Septal Defect
Norethindrone Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Norethindrone adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!