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Lendormin adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 11. View All

Lendormin FDA safety alerts: No

Reported hospitalizations: 5

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

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6100525-7 | Rash Scarlatiniform
on Feb 24, 2009 Female patient from JAPAN , weighting 113.3 lb, was diagnosed with insomnia, pruritus, reflux oesophagitis, cerebral infarction, shunt occlusion, renal failure chronic and was treated with Lendormin (View Usage). Patient experienced the following unwanted or unexpected effects: rash scarlatiniform. Lendormin dosage: . During the same period patient was treated with ALLEGRA (View Allegra Review and Allegra Label ), TAKEPRON (View Takepron Review and Takepron Label ), PLAVIX (View Plavix Review and Plavix Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

6080871-6 | Rash Scarlatiniform
Patient was taking Lendormin (View Usage). Patient had the following side effects: rash scarlatiniform on Feb 11, 2009 from JAPAN Additional patient health information: Female patient , weighting 113.3 lb, was diagnosed with pruritus, reflux oesophagitis, cerebral infarction, shunt occlusion, renal failure chronic and. Lendormin dosage: . During the same period patient was treated with ALLEGRA (View Allegra Review and Allegra Label ), TAKEPRON (View Takepron Review and Takepron Label ), PLAVIX (View Plavix Review and Plavix Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

6074214-1 | Anastomotic Complication, Hypoaesthesia, Hypoaesthesia Oral
Adverse event was reported on Jan 30, 2009 by a Male patient taking Lendormin (View Usage) (Dosage: ) was diagnosed with colon cancer recurrent and. Location: JAPAN , weighting 110.2 lb, After Lendormin was administered, patient had the following side effects: anastomotic complication, hypoaesthesia, hypoaesthesia oral. During the same period patient was treated with AVASTIN (View Avastin Review and Avastin Label ), CALCIUM LEVOFOLINATE (300 Mg) (View Calcium Levofolinate Review and Calcium Levofolinate Label ), FLUOROURACIL (625 Mg) (View Fluorouracil Review and Fluorouracil Label ), ELPLAT (130 Mg) (View Elplat Review and Elplat Label ).

5708008-0 | Dyskinesia
on Apr 04, 2008 Male patient from JAPAN , 77 years of age, was treated with Lendormin (View Usage). Patient experienced the following unwanted or unexpected effects: dyskinesia. Lendormin dosage: 0.25 Mg. During the same period patient was treated with HALCION (0.25 Mg) (View Halcion Review and Halcion Label ), EVAMYL (2 Mg) (View Evamyl Review and Evamyl Label ), AMOBAN (7.5 Mg) (View Amoban Review and Amoban Label ), MYSLEE (10 Mg) (View Myslee Review and Myslee Label ).


5367601-8 | Interstitial Lung Disease
on Jun 12, 2007 Female patient from JAPAN , 46 years of age, was treated with Lendormin (View Usage). Patient had the following side effects: interstitial lung disease. Lendormin dosage: Unk. During the same period patient was treated with ZOLPIDEM (10 Mg) (View Zolpidem Review and Zolpidem Label ).

5115208-X | Fatigue, Suicide Attempt
Patient was taking Lendormin (View Usage). After Lendormin was administered, patient had the following side effects: fatigue, suicide attempt on Sep 20, 2006 from GERMANY Additional patient health information: Female patient , weighting 154.3 lb, . Lendormin dosage: . During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ). Patient was hospitalized.

4868277-6 | Hepatitis
Adverse event was reported on Nov 30, 2005 by a Female patient taking Lendormin (View Usage) (Dosage: ) . Location: JAPAN , 62 years of age, Patient experienced the following unwanted or unexpected effects: hepatitis (What is hepatitis?). During the same period patient was treated with PEPCID RPD (View Pepcid Rpd Review and Pepcid Rpd Label ), BONZOL (View Bonzol Review and Bonzol Label ), GASMOTIN (View Gasmotin Review and Gasmotin Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), SENNOSIDES (View Sennosides Review and Sennosides Label ).

4811771-4 | Rhabdomyolysis
on Oct 21, 2005 Male patient from JAPAN , 50 years of age, was diagnosed with ill-defined disorder and was treated with Lendormin (View Usage). Patient had the following side effects: rhabdomyolysis. Lendormin dosage: Daily Dose: 1 Milligram(s). During the same period patient was treated with LUVOX (Daily Dose: 75 Milligram(s)) (View Luvox Review and Luvox Label ), DEPAS (Daily Dose: 1 Milligram(s)) (View Depas Review and Depas Label ).

4754119-6 | Erythema, Haematocrit Decreased, Lymphocyte Count Decreased, Lymphocyte Percentage Decreased, Monocyte Percentage Decreased, Platelet Count Decreased, Red Blood Cell Count Decreased, Skin Test Positive
on Jul 20, 2005 Male patient from JAPAN , 70 years of age, weighting 158.7 lb, was diagnosed with insomnia, sputum retention, hypertension, postoperative infection, bacterial sepsis, gastric disorder and was treated with Lendormin (View Usage). After Lendormin was administered, patient had the following side effects: erythema, haematocrit decreased, lymphocyte count decreased, lymphocyte percentage decreased, monocyte percentage decreased, platelet count decreased, red blood cell count decreased, skin test positive. Lendormin dosage: . During the same period patient was treated with BROMHEXINE HYDROCHLORIDE (View Bromhexine Hydrochloride Review and Bromhexine Hydrochloride Label ), NORVASC (View Norvasc Review and Norvasc Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), PRIMAXIN (View Primaxin Review and Primaxin Label ), VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), BIOFERMIN (View Biofermin Review and Biofermin Label ).

4564008-8 | Femoral Neck Fracture, Insomnia, Metastases To Bone, Metastases To Spine, Pain In Extremity
Patient was taking Lendormin (View Usage). Patient experienced the following unwanted or unexpected effects: femoral neck fracture, insomnia, metastases to bone, metastases to spine, pain in extremity on Dec 01, 2004 from Additional patient health information: Male patient , 73 years of age, weighting 154.3 lb, was diagnosed with insomnia, pain (What is pain?), polyuria, prostate cancer metastatic, gastric ulcer and. Lendormin dosage: . During the same period patient was treated with MORPHINE SULFATE (View Morphine Sulfate Review and Morphine Sulfate Label ), LASIX (View Lasix Review and Lasix Label ), DECADRON (View Decadron Review and Decadron Label ), GASTER (View Gaster Review and Gaster Label ), CATLEP (View Catlep Review and Catlep Label ). Patient was hospitalized and became disabled.

4556430-0 | Abasia, Asthenia, Blood Creatinine Increased, Blood Urea Increased, Cerebrovascular Disorder, Epilepsy, Eye Movement Disorder, Oliguria, Pain
Adverse event was reported on Dec 22, 2003 by a Male patient taking Lendormin (View Usage) (Dosage: 3 Df/d) was diagnosed with nail tinea and. Location: , 74 years of age, Patient had the following side effects: abasia, asthenia, blood creatinine increased, blood urea increased, cerebrovascular disorder, epilepsy (What is epilepsy?), eye movement disorder, oliguria, pain (What is pain?). During the same period patient was treated with LOXONIN (3 Df/d) (View Loxonin Review and Loxonin Label ), ARTIST (20 Mg/d) (View Artist Review and Artist Label ), GASTER D (20 Mg/d) (View Gaster D Review and Gaster D Label ), ZYRTEC (1 Df, Qd) (View Zyrtec Review and Zyrtec Label ), LAMISIL (125 Mg, Qd) (View Lamisil Review and Lamisil Label ), EBASTEL (1 Df, Qd) (View Ebastel Review and Ebastel Label ), SIGMART (10 Mg/d) (View Sigmart Review and Sigmart Label ), MYONAL (150 Mg/d) (View Myonal Review and Myonal 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 Lendormin 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 Lendormin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lendormin 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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Lendormin Reactions
Abasia
Anastomotic Complication
Asthenia
Blood Creatinine Increased
Blood Urea Increased
Cerebrovascular Disorder
Dyskinesia
EpilepsyWhat is Epilepsy?
Erythema
Eye Movement Disorder
Fatigue
Femoral Neck Fracture
Haematocrit Decreased
HepatitisWhat is Hepatitis?
Hypoaesthesia
Hypoaesthesia Oral
Insomnia
Interstitial Lung Disease
Lymphocyte Count Decreased
Lymphocyte Percentage Decreased
Metastases To Bone
Metastases To Spine
Monocyte Percentage Decreased
Oliguria
PainWhat is Pain?
Pain In Extremity
Platelet Count Decreased
Rash Scarlatiniform
Red Blood Cell Count Decreased
Rhabdomyolysis
Lendormin 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 Lendormin 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!