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Doxepin adverse events reported to FDA.

Have You Experienced unusual Doxepin symptoms? PatientsVille.com collects and analyzes Doxepin side effect and adverse reports submitted by Doxepin users, such as neuropathy |.

Summary

FDA Adverse Reports: 7. View All

Doxepin FDA safety alerts: No

Reported deaths: 94

Reported hospitalizations: 31

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Often additional risks of using a medication, such as Doxepin, 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 Doxepin users, Learn more about unwanted side effects & find ways to reduce them. Browse Doxepin Adverse Reports reported to FDA and participate in Doxepin discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Doxepin. 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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Doxepin Adverse Effect Reports (FDA)

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4792006-8 | Cardio-respiratory Arrest, Completed Suicide, Overdose
on Sep 19, 2005 Female patient from UNITED STATES , 55 years of age, was treated with Doxepin (View Usage). Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, completed suicide, overdose. Doxepin dosage: Df Unk Po. During the same period patient was treated with METHADONE (Df Unk Po) (View Methadone Review and Methadone Label ).

4792005-6 | Cardio-respiratory Arrest, Completed Suicide, Overdose
Patient was taking Doxepin (View Usage). Patient had the following side effects: cardio-respiratory arrest, completed suicide, overdose on Sep 19, 2005 from UNITED STATES Additional patient health information: Female patient , 48 years of age, . Doxepin dosage: Df Unk Po. During the same period patient was treated with METHADONE (Df Unk Po) (View Methadone Review and Methadone Label ).

4792004-4 | Completed Suicide, Overdose
Adverse event was reported on Sep 19, 2005 by a Female patient taking Doxepin (View Usage) (Dosage: Df Unk Po) . Location: UNITED STATES , 57 years of age, After Doxepin was administered, patient had the following side effects: completed suicide, overdose. During the same period patient was treated with ENALAPRIL (Df Unk Po) (View Enalapril Review and Enalapril Label ), RISPERIDONE (Df Unk Po) (View Risperidone Review and Risperidone Label ).

4792003-2 | Completed Suicide, Overdose
on Sep 19, 2005 Female patient from UNITED STATES , 57 years of age, was treated with Doxepin (View Usage). Patient experienced the following unwanted or unexpected effects: completed suicide, overdose. Doxepin dosage: Df Unk Po. During the same period patient was treated with BENZODIAZEPINE (Df Unk Po) (View Benzodiazepine Review and Benzodiazepine Label ), HYDROCHLOROTHIAZIDE W/VALSARTAN (Df Unk Po) (View Hydrochlorothiazide W/valsartan Review and Hydrochlorothiazide W/valsartan Label ).


4792002-0 | Completed Suicide
on Sep 19, 2005 Female patient from UNITED STATES , 50 years of age, was treated with Doxepin (View Usage). Patient had the following side effects: completed suicide. Doxepin dosage: Df Unk Po. During the same period patient was treated with ESCITALOPRAM (Df Unk Po) (View Escitalopram Review and Escitalopram Label ), METOPROLOL (Df Unk Po) (View Metoprolol Review and Metoprolol Label ).

4792001-9 | Completed Suicide, Overdose
Patient was taking Doxepin (View Usage). After Doxepin was administered, patient had the following side effects: completed suicide, overdose on Sep 19, 2005 from UNITED STATES Additional patient health information: Female patient , 40 years of age, . Doxepin dosage: Df Unk Po. During the same period patient was treated with QUETIAPINE FUMARATE (Df Unk Po) (View Quetiapine Fumarate Review and Quetiapine Fumarate Label ), CLONAZEPAM (Df Unk Po) (View Clonazepam Review and Clonazepam Label ).

4788527-4 | Depressed Level Of Consciousness, Electrocardiogram Qrs Complex Prolonged, Lethargy, Overdose, Tachypnoea
Adverse event was reported on Oct 05, 2005 by a Male patient taking Doxepin (View Usage) (Dosage: ) . Location: UNITED STATES , 55 years of age, Patient experienced the following unwanted or unexpected effects: depressed level of consciousness, electrocardiogram qrs complex prolonged, lethargy, overdose, tachypnoea. During the same period patient was treated with METOPROLOL (View Metoprolol Review and Metoprolol Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ), PHENYTOIN (View Phenytoin Review and Phenytoin Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), OLANZAPINE (View Olanzapine Review and Olanzapine Label ). Patient was hospitalized.


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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 Doxepin 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 Doxepin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Doxepin 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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Doxepin 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 Doxepin 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!