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Quasense adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 13. View All

Quasense FDA safety alerts: No

Reported hospitalizations: 4

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

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6094055-9 | Menorrhagia, Migraine
on Feb 24, 2009 Female patient from UNITED STATES , weighting 160.0 lb, was diagnosed with contraception, menstrual disorder and was treated with Quasense (View Usage). Patient experienced the following unwanted or unexpected effects: menorrhagia, migraine (What is migraine?). Quasense dosage: One Pill One Time A Day Po.

6045144-6 | Deep Vein Thrombosis
Patient was taking Quasense (View Usage). Patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?) on Jan 16, 2009 from UNITED STATES Additional patient health information: Female patient , 40 years of age, weighting 246.9 lb, was diagnosed with contraception and. Quasense dosage: 1 Pill Daily Po. Patient was hospitalized.

5897489-8 | Accidental Exposure, Cholelithiasis, Hepatotoxicity, Liver Injury, Urinary Tract Infection
Adverse event was reported on Sep 24, 2008 by a Female patient taking Quasense (View Usage) (Dosage: ) . Location: UNITED STATES , 23 years of age, After Quasense was administered, patient had the following side effects: accidental exposure, cholelithiasis, hepatotoxicity, liver injury, urinary tract infection (What is urinary tract infection?). During the same period patient was treated with BACTRIM (View Bactrim Review and Bactrim Label ).

5872003-1 | Affective Disorder, Blood Pressure Increased, Fatigue, Feeling Abnormal, Sinusitis, Stress
on Sep 04, 2008 Female patient from UNITED STATES , 36 years of age, weighting 164.0 lb, was diagnosed with contraception and was treated with Quasense (View Usage). Patient experienced the following unwanted or unexpected effects: affective disorder, blood pressure increased, fatigue, feeling abnormal, sinusitis (What is sinusitis?), stress (What is stress?). Quasense dosage: 1 Tablet Q Day Po.


5757903-5 | Breast Enlargement, Metrorrhagia, Mood Swings, Muscle Spasms, Weight Increased
on Jun 03, 2008 Female patient from UNITED STATES , 32 years of age, weighting 130.0 lb, was diagnosed with contraception, endometriosis (What is endometriosis?) and was treated with Quasense (View Usage). Patient had the following side effects: breast enlargement, metrorrhagia, mood swings, muscle spasms, weight increased. Quasense dosage: 1 Tab Qd Po.

5729097-3 | Muscle Spasms
Patient was taking Quasense (View Usage). After Quasense was administered, patient had the following side effects: muscle spasms on May 05, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 203.0 lb, was diagnosed with contraception and. Quasense dosage: 1 Po Q Day.

5562973-3 | Abdominal Distension, Depression, Fatigue, Irritability, Libido Decreased, Muscle Spasms, Thinking Abnormal, Weight Increased
Adverse event was reported on Dec 12, 2007 by a Female patient taking Quasense (View Usage) (Dosage: One Tablet Per Day 3 Months Po) was diagnosed with contraception and. Location: UNITED STATES , 45 years of age, weighting 138.0 lb, Patient experienced the following unwanted or unexpected effects: abdominal distension, depression (What is depression?), fatigue, irritability, libido decreased, muscle spasms, thinking abnormal, weight increased.

5500703-1 | Complex Partial Seizures, Grand Mal Convulsion
on Oct 16, 2007 Female patient from UNITED STATES , 43 years of age, was diagnosed with convulsion, complex partial seizures and was treated with Quasense (View Usage). Patient had the following side effects: complex partial seizures, grand mal convulsion. Quasense dosage: 1 Tablet Daily; Oral. During the same period patient was treated with LAMICTAL (300 Mg, Qam/qpm,) (View Lamictal Review and Lamictal Label ), KEPPRA (View Keppra Review and Keppra Label ). Patient was hospitalized.

5490032-7 | Complex Partial Seizures, Nervousness, Unevaluable Event
on Oct 02, 2007 Female patient from UNITED STATES , 43 years of age, was diagnosed with convulsion, complex partial seizures and was treated with Quasense (View Usage). After Quasense was administered, patient had the following side effects: complex partial seizures, nervousness, unevaluable event. Quasense dosage: 1 Tablet, Daily, Oral. During the same period patient was treated with LAMICTAL (300 Mg,qam/qpm) (View Lamictal Review and Lamictal Label ), KEPPRA (View Keppra Review and Keppra Label ). Patient was hospitalized.

5273648-2 | Deep Vein Thrombosis, Eye Disorder, Migraine, Pulmonary Embolism, Visual Disturbance
Patient was taking Quasense (View Usage). Patient experienced the following unwanted or unexpected effects: deep vein thrombosis (What is deep vein thrombosis?), eye disorder, migraine (What is migraine?), pulmonary embolism (What is pulmonary embolism?), visual disturbance on Mar 21, 2007 from UNITED STATES Additional patient health information: Female patient , 30 years of age, weighting 172.0 lb, was diagnosed with contraception and. Quasense dosage: 91-day Regimen Once Daily Po. Patient was hospitalized.

5233350-X | Metrorrhagia, Muscle Spasms
Adverse event was reported on Feb 06, 2007 by a Female patient taking Quasense (View Usage) (Dosage: One Daily X Every Day Po) was diagnosed with haemorrhage, muscle spasms and. Location: UNITED STATES , 50 years of age, weighting 170.0 lb, Patient had the following side effects: metrorrhagia, muscle spasms. During the same period patient was treated with SEASONALE (One Daily X Every Day Po) (View Seasonale Review and Seasonale Label ).

5175271-7 | Nausea
on Dec 11, 2006 Female patient from UNITED STATES , 16 years of age, was diagnosed with haemorrhage and was treated with Quasense (View Usage). After Quasense was administered, patient had the following side effects: nausea (What is nausea?). Quasense dosage: Take One Tablet Daily.

5151016-1 | Vaginal Haemorrhage
on Nov 13, 2006 Female patient from UNITED STATES , 18 years of age, weighting 145.0 lb, was diagnosed with haemorrhage and was treated with Quasense (View Usage). Patient experienced the following unwanted or unexpected effects: vaginal haemorrhage. Quasense dosage: Orally Daily. During the same period patient was treated with ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), SINGULAIR (View Singulair Review and Singulair Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ).


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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 Quasense 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 Quasense quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Quasense 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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Deep vein thrombosis, or DVT, is a blood clot that forms in

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Quasense Reactions
Abdominal Distension
Accidental Exposure
Affective Disorder
Blood Pressure Increased
Breast Enlargement
Cholelithiasis
Complex Partial Seizures
Deep Vein ThrombosisWhat is Deep vein thrombosis?
DepressionWhat is Depression?
Eye Disorder
Fatigue
Feeling Abnormal
Grand Mal Convulsion
Hepatotoxicity
Irritability
Libido Decreased
Liver Injury
Menorrhagia
Metrorrhagia
MigraineWhat is Migraine?
Mood Swings
Muscle Spasms
NauseaWhat is Nausea?
Nervousness
Pulmonary EmbolismWhat is Pulmonary embolism?
SinusitisWhat is Sinusitis?
StressWhat is Stress?
Thinking Abnormal
Thrombosis
Weight Increased
Quasense 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 Quasense 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!