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If You had Imovane side effect, You are not alone. Other patients reported side effects.
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Frenquency Micturition (2)
Imovane (2)
Interdose Withdrawal (2)
Depression (1)
Hunger Pains At Night (1)
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Common Imovane Side Effects

top 5 Imovane|Frenquency|Imovane|Interdose |Depression|Hunger pai adverse effects>>See All Imovane Side Effects

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Imovane adverse events reported to FDA.

Have You Experienced unusual Imovane symptoms? PatientsVille.com collects and analyzes Imovane side effect and adverse reports submitted by Imovane users, such as Burning in throat. Feels like something is|.

Summary

FDA Adverse Reports: 14. View All

Imovane FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 9

More About Imovane

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1Imovane
2Interdose Withdrawal
3Hunger Pains At Night
4Frenquency Micturition
5Depression
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Burning in throat. Feels like something is

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

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6763646-1 | International Normalised Ratio Increased, Prothrombin Level Decreased
on May 28, 2010 Male patient from FRANCE , 41 years of age, was diagnosed with insomnia, anxiety (What is anxiety?) and was treated with Imovane (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased, prothrombin level decreased. Imovane dosage: . During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), METHADONE (View Methadone Review and Methadone Label ), ATARAX (View Atarax Review and Atarax Label ), PREVISCAN (View Previscan Review and Previscan Label ), ALDACTONE (View Aldactone Review and Aldactone Label ). Patient was hospitalized.

6762125-5 | Hellp Syndrome
Patient was taking Imovane (View Usage). Patient had the following side effects: hellp syndrome on May 28, 2010 from FRANCE Additional patient health information: Female patient , 40 years of age, . Imovane dosage: . During the same period patient was treated with LARGACTIL (Dose:60 Unit(s)) (View Largactil Review and Largactil Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ), NEULEPTIL (Dose:50 Unit(s)) (View Neuleptil Review and Neuleptil Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), LEXOMIL (View Lexomil Review and Lexomil Label ), RIVOTRIL (Dose:2 Unit(s)) (View Rivotril Review and Rivotril Label ). Patient was hospitalized.

6018169-4 | Cholestatic Liver Injury, Hepatocellular Injury, Jaundice
Adverse event was reported on Dec 12, 2008 by a Male patient taking Imovane (View Usage) (Dosage: ) . Location: , 72 years of age, After Imovane was administered, patient had the following side effects: cholestatic liver injury, hepatocellular injury, jaundice (What is jaundice?). During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), OFLOCET /00731801/ (View Oflocet /00731801/ Review and Oflocet /00731801/ Label ), DI ANTALVIC /00220901/ (View Di-antalvic /00220901/ Review and Di-antalvic /00220901/ Label ), TAVANIC (View Tavanic Review and Tavanic Label ), CRESTOR (View Crestor Review and Crestor Label ), PREVISCAN /00789001/ (View Previscan /00789001/ Review and Previscan /00789001/ Label ). Patient was hospitalized.

5645665-1 | Amnesia, Anxiety, Confusional State, Fall, Somnambulism, Visual Acuity Reduced, Weight Decreased
on Feb 19, 2008 Female patient from AUSTRALIA , 30 years of age, was diagnosed with insomnia and was treated with Imovane (View Usage). Patient experienced the following unwanted or unexpected effects: amnesia, anxiety (What is anxiety?), confusional state, fall (What is fall?), somnambulism, visual acuity reduced, weight decreased. Imovane dosage: Unk. During the same period patient was treated with STILNOX (Unk) (View Stilnox Review and Stilnox Label ).


5331124-2 | Toxic Epidermal Necrolysis
on May 10, 2007 Male patient from , 22 years of age, was treated with Imovane (View Usage). Patient had the following side effects: toxic epidermal necrolysis. Imovane dosage: . During the same period patient was treated with DEPAKENE (View Depakene Review and Depakene Label ), DI HYDAN (View Di-hydan Review and Di-hydan Label ), FORTUM /00559702/ (View Fortum /00559702/ Review and Fortum /00559702/ Label ), LOVENOX (View Lovenox Review and Lovenox Label ), FORLAX (View Forlax Review and Forlax Label ). Patient was hospitalized.

5215598-3 | Headache, Heart Rate Increased, Laryngospasm, Mydriasis, Somnolence, Status Epilepticus
Patient was taking Imovane (View Usage). After Imovane was administered, patient had the following side effects: headache (What is headache?), heart rate increased, laryngospasm, mydriasis, somnolence, status epilepticus on Jan 15, 2007 from FRANCE Additional patient health information: Female patient , 83 years of age, . Imovane dosage: 3.75 Mg, Qd. During the same period patient was treated with EXELON (1.5 Mg, Bid) (View Exelon Review and Exelon Label ), ACETAMINOPHEN AND TRAMADOL HCL (325/37.5 Mg, Tid) (View Acetaminophen And Tramadol Hcl Review and Acetaminophen And Tramadol Hcl Label ). Patient was hospitalized.

5033651-4 | Confusional State, Hypoglycaemia, Malaise, Syncope
Adverse event was reported on Jun 19, 2006 by a Female patient taking Imovane (View Usage) (Dosage: Unk) . Location: FRANCE , 88 years of age, weighting 110.2 lb, Patient experienced the following unwanted or unexpected effects: confusional state, hypoglycaemia, malaise, syncope. During the same period patient was treated with DOLIPRANE (Unk) (View Doliprane Review and Doliprane Label ), VITAMINE D (Unk) (View Vitamine D Review and Vitamine D Label ), CALCIDOSE (Unk) (View Calcidose Review and Calcidose Label ), ADANCOR (20 Mg) (View Adancor Review and Adancor Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), LEXOMIL (Unk) (View Lexomil Review and Lexomil Label ), VASTAREL (70 Mg) (View Vastarel Review and Vastarel Label ), APROVEL (View Aprovel Review and Aprovel Label ). Patient was hospitalized.

4979031-9 | Abortion Spontaneous
on Feb 22, 2006 Female patient from CANADA , 36 years of age, was diagnosed with irritable bowel syndrome (What is irritable bowel syndrome?) and was treated with Imovane (View Usage). Patient had the following side effects: abortion spontaneous. Imovane dosage: 1/2 Tablet From Time To Time. During the same period patient was treated with ZELNORM (1 Tablet Per Day, Not Every Day) (View Zelnorm Review and Zelnorm Label ).

4962856-3 | Food Allergy, Hyperthermia, Joint Sprain, Rash, Respiratory Disorder, Stomatitis
on Mar 30, 2006 Female patient from FRANCE , 79 years of age, weighting 119.0 lb, was diagnosed with ill-defined disorder, essential hypertension, epilepsy (What is epilepsy?), stomatitis and was treated with Imovane (View Usage). After Imovane was administered, patient had the following side effects: food allergy (What is food allergy?), hyperthermia, joint sprain, rash (What is rash?), respiratory disorder, stomatitis. Imovane dosage: . During the same period patient was treated with COVERSYL (Daily Dose: 2 Milligram(s)) (View Coversyl Review and Coversyl Label ), LAMOTRIGINE (View Lamotrigine Review and Lamotrigine Label ), KARDEGIC (Daily Dose: 75 Milligram(s)) (View Kardegic Review and Kardegic Label ), DEPAKENE (Daily Dose: 750 Milligram(s)) (View Depakene Review and Depakene Label ), MOTILIUM (View Motilium Review and Motilium Label ), RULID (View Rulid Review and Rulid Label ), LANZOR (Daily Dose: 30 Milligram(s)) (View Lanzor Review and Lanzor Label ). Patient was hospitalized.

4916953-9 | Dehydration, Fall, Food Intolerance, Incontinence, Mobility Decreased, Orthostatic Hypotension, Renal Failure, Sinus Bradycardia
Patient was taking Imovane (View Usage). Patient experienced the following unwanted or unexpected effects: dehydration, fall (What is fall?), food intolerance, incontinence, mobility decreased, orthostatic hypotension, renal failure, sinus bradycardia on Feb 09, 2006 from FRANCE Additional patient health information: Female patient , 78 years of age, was diagnosed with ill-defined disorder, hypertension, hypertensive cardiomyopathy and. Imovane dosage: . During the same period patient was treated with COVERSYL (Daily Dose: 4 Milligram(s)) (View Coversyl Review and Coversyl Label ), DEPAKOTE (View Depakote Review and Depakote Label ), CARDENSIEL (View Cardensiel Review and Cardensiel Label ), KETOPROFEN (View Ketoprofen Review and Ketoprofen Label ), LASILIX (View Lasilix Review and Lasilix Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ), CALCIDOSE (View Calcidose Review and Calcidose Label ), OXYBUTYNIN (View Oxybutynin Review and Oxybutynin Label ). Patient was hospitalized.

4903681-9 | Cardiac Arrest, Condition Aggravated, Erythema Multiforme, Extremity Necrosis, Finger Amputation, Gamma-glutamyltransferase Increased, Haemodialysis, Hand Amputation, Hepatic Enzyme Increased
Adverse event was reported on May 02, 2005 by a Female patient taking Imovane (View Usage) (Dosage: ) was diagnosed with septic shock and. Location: , 48 years of age, weighting 132.3 lb, Patient had the following side effects: cardiac arrest (What is cardiac arrest?), condition aggravated, erythema multiforme, extremity necrosis, finger amputation, gamma-glutamyltransferase increased, haemodialysis, hand amputation, hepatic enzyme increased. During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), CORDARONE (View Cordarone Review and Cordarone Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), AMIKACIN (View Amikacin Review and Amikacin Label ).

4678256-X | Condition Aggravated, Erythema Multiforme, Finger Amputation, Gamma-glutamyltransferase Increased, Haemodialysis, Hand Amputation, Hepatic Enzyme Increased, Leg Amputation, Renal Failure
on May 02, 2005 Female patient from , 48 years of age, weighting 132.3 lb, was diagnosed with septic shock and was treated with Imovane (View Usage). After Imovane was administered, patient had the following side effects: condition aggravated, erythema multiforme, finger amputation, gamma-glutamyltransferase increased, haemodialysis, hand amputation, hepatic enzyme increased, leg amputation, renal failure. Imovane dosage: . During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), CORDARONE (View Cordarone Review and Cordarone Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), AMIKACIN (View Amikacin Review and Amikacin Label ).

4653320-X | Condition Aggravated, Erythema Multiforme, Toxic Epidermal Necrolysis
on May 02, 2005 Female patient from , 48 years of age, weighting 132.3 lb, was diagnosed with septic shock and was treated with Imovane (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, erythema multiforme, toxic epidermal necrolysis. Imovane dosage: . During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), CORDARONE (View Cordarone Review and Cordarone Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), AMIKACIN (View Amikacin Review and Amikacin Label ).

4614724-4 | Bronchitis, Influenza Like Illness, Renal Failure
Patient was taking Imovane (View Usage). Patient had the following side effects: bronchitis (What is bronchitis?), influenza like illness, renal failure on Mar 07, 2005 from Additional patient health information: Female patient , 94 years of age, was diagnosed with ill-defined disorder and. Imovane dosage: . During the same period patient was treated with COVERSYL (View Coversyl Review and Coversyl Label ). Patient was hospitalized.


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Imovane Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

Robert   Somerset 

4:31am on Monday, December 14th, 2009

I dont know if anyone is aware - but i was diagnosed as having an alergy to dust mites, no taste and... read more »

jeannette bibollet   annecy 

7:49am on Sunday, August 9th, 2009

how to stop imovane and be able to sleep normally?

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 Imovane 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 Imovane quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Imovane 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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Imovane Reactions
Abortion Spontaneous
Amnesia
AnxietyWhat is Anxiety?
BronchitisWhat is Bronchitis?
Cardiac ArrestWhat is Cardiac arrest?
Cholestatic Liver Injury
Condition Aggravated
Confusional State
Dehydration
Erythema Multiforme
Extremity Necrosis
FallWhat is Fall?
Finger Amputation
Food AllergyWhat is Food allergy?
Food Intolerance
Gamma-glutamyltransferase Increased
Haemodialysis
Hand Amputation
HeadacheWhat is Headache?
Heart Rate Increased
Hellp Syndrome
Hepatic Enzyme Increased
Hepatocellular Injury
Hyperthermia
Hypoglycaemia
Incontinence
Influenza Like Illness
International Normalised Ratio Increased
Renal Failure
Toxic Epidermal Necrolysis
Imovane 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 Imovane 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!