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Leuplin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Leuplin FDA safety alerts: No

Reported deaths: 215

Reported hospitalizations: 155

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

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5170036-4 | Cerebral Artery Stenosis, Drooling, Fall, Gait Disturbance, Oedema Peripheral, Platelet Count Decreased, Pleural Effusion, Pneumonia, Pyrexia
on Oct 31, 2006 Male patient from JAPAN , 81 years of age, weighting 154.3 lb, was diagnosed with prostate cancer (What is prostate cancer?), constipation (What is constipation?), hypertension, back pain (What is back pain?), stomach discomfort, dysuria and was treated with Leuplin (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral artery stenosis, drooling, fall (What is fall?), gait disturbance, oedema peripheral, platelet count decreased, pleural effusion, pneumonia (What is pneumonia?), pyrexia. Leuplin dosage: 11.25 Mg, Other. During the same period patient was treated with MAGNESIUM OXIDE (660 Mg, 3/d) (View Magnesium Oxide Review and Magnesium Oxide Label ), BLOPRESS /GFR/ (8 Mg, Daily (1/d)) (View Blopress /gfr/ Review and Blopress /gfr/ Label ), OSTELUC (200 Mg, 2/d) (View Osteluc Review and Osteluc Label ), GASMOTIN (5 Mg, 3/d) (View Gasmotin Review and Gasmotin Label ), HARNAL (View Harnal Review and Harnal Label ), PURSENNID /SCH/ (36 Mg, Other) (View Pursennid /sch/ Review and Pursennid /sch/ Label ), UBRETID (5 Mg, Daily (1/d)) (View Ubretid Review and Ubretid Label ), ADALAT CR /THA/ (20 Mg, Daily (1/d)) (View Adalat Cr /tha/ Review and Adalat Cr /tha/ Label ). Patient was hospitalized and became disabled.

5161817-1 | Cerebral Artery Stenosis, Drooling, Fall, Gait Disturbance, Oedema Peripheral, Platelet Count Decreased, Pleural Effusion, Pneumonia, Pyrexia
Patient was taking Leuplin (View Usage). Patient had the following side effects: cerebral artery stenosis, drooling, fall (What is fall?), gait disturbance, oedema peripheral, platelet count decreased, pleural effusion, pneumonia (What is pneumonia?), pyrexia on Oct 31, 2006 from JAPAN Additional patient health information: Male patient , 81 years of age, weighting 154.3 lb, was diagnosed with prostate cancer (What is prostate cancer?), constipation (What is constipation?), hypertension, back pain (What is back pain?), stomach discomfort, dysuria and. Leuplin dosage: 11.25 Mg, Other. During the same period patient was treated with MAGNESIUM OXIDE (660 Mg, 3/d) (View Magnesium Oxide Review and Magnesium Oxide Label ), BLOPRESS /GFR/ (8 Mg, Daily (1/d)) (View Blopress /gfr/ Review and Blopress /gfr/ Label ), OSTELUC (200 Mg, 2/d) (View Osteluc Review and Osteluc Label ), GASMOTIN (5 Mg, 3/d) (View Gasmotin Review and Gasmotin Label ), HARNAL (View Harnal Review and Harnal Label ), PURSENNID /SCH/ (36 Mg, Other) (View Pursennid /sch/ Review and Pursennid /sch/ Label ), UBRETID (5 Mg, Daily (1/d)) (View Ubretid Review and Ubretid Label ), ADALAT CR /THA/ (20 Mg, Daily (1/d)) (View Adalat Cr /tha/ Review and Adalat Cr /tha/ Label ). Patient was hospitalized and became disabled.

4907430-X | Acute Respiratory Distress Syndrome, Asthenia, Blood Pressure Decreased, Blood Pressure Systolic Increased, Bronchial Disorder, Disseminated Intravascular Coagulation, Electrolyte Imbalance, Hypokalaemia, Hypoxia
Adverse event was reported on Feb 03, 2006 by a Male patient taking Leuplin (View Usage) (Dosage: 3.75 Mg (3.75 Mg 1 In 28d)) was diagnosed with prostate cancer (What is prostate cancer?) and. Location: JAPAN , 81 years of age, After Leuplin was administered, patient had the following side effects: acute respiratory distress syndrome, asthenia, blood pressure decreased, blood pressure systolic increased, bronchial disorder, disseminated intravascular coagulation, electrolyte imbalance, hypokalaemia, hypoxia. During the same period patient was treated with GASPORT (FAMOTIDINE) (View Gasport (famotidine) Review and Gasport (famotidine) Label ), PIETENALE (TICLOPIDINE HYDROCHLORIDE) (View Pietenale (ticlopidine Hydrochloride) Review and Pietenale (ticlopidine Hydrochloride) Label ), MARZULENE S (MARZULENE S) (GRANULATE) (View Marzulene S (marzulene S) (granulate) Review and Marzulene S (marzulene S) (granulate) Label ), JIRUSTAN L (CHLORMADINONE ACETATE) (View Jirustan L (chlormadinone Acetate) Review and Jirustan L (chlormadinone Acetate) Label ), SATANOLOL (DIFENIDOL HYDROCHLORIDE) (View Satanolol (difenidol Hydrochloride) Review and Satanolol (difenidol Hydrochloride) Label ), ................. (View ................. Review and ................. Label ), .................. (View .................. Review and .................. Label ), ........................ (View ........................ Review and ........................ Label ). Patient was hospitalized.

4664913-8 | Blood Alkaline Phosphatase Increased, Hepatic Function Abnormal, Liver Disorder, Pneumonia
on May 13, 2005 Male patient from , 82 years of age, was diagnosed with prostate cancer (What is prostate cancer?) and was treated with Leuplin (View Usage). Patient experienced the following unwanted or unexpected effects: blood alkaline phosphatase increased, hepatic function abnormal, liver disorder, pneumonia (What is pneumonia?). Leuplin dosage: 3.75 Mg (3.75 Mg, 1 In 28 D). During the same period patient was treated with FLUTAMIDE (375 Mg (375 Mg, 1 D)) (View Flutamide Review and Flutamide Label ). Patient was hospitalized.


4576336-0 | Arterial Thrombosis Limb, Difficulty In Walking, Genital Haemorrhage, Hypoaesthesia, Inadequate Analgesia, Insomnia, Myalgia, Pain, Pain In Extremity
on Feb 01, 2005 Female patient from , 49 years of age, was diagnosed with menorrhagia and was treated with Leuplin (View Usage). Patient had the following side effects: arterial thrombosis limb, difficulty in walking, genital haemorrhage, hypoaesthesia, inadequate analgesia, insomnia, myalgia, pain (What is pain?), pain in extremity. Leuplin dosage: 3.75 Mg (3.75 Mg, 1 In 28 D) Subcutaneous. During the same period patient was treated with PANOVAR (ETHINYL ESTRADIOL W/NORGESTREL) (TABLETS) (2 Tab. (1 Tab. 2 In 1 D) Per Oral) (View Panovar (ethinyl Estradiol W/norgestrel) (tablets) Review and Panovar (ethinyl Estradiol W/norgestrel) (tablets) Label ), PLANOVAR (ETHINYL ESTRADIOL W/NORGESTREL) (TABLETS) (1 Tab (1 Tab. In 1 D) Per Oral) (View Planovar (ethinyl Estradiol W/norgestrel) (tablets) Review and Planovar (ethinyl Estradiol W/norgestrel) (tablets) Label ), FERROMIA (FERROUS CITRATE) (View Ferromia (ferrous Citrate) Review and Ferromia (ferrous Citrate) Label ), ......... (View ......... Review and ......... Label ), CINAL (CINAL) (View Cinal (cinal) Review and Cinal (cinal) 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 Leuplin 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 Leuplin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Leuplin 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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Leuplin Reactions
Acute Respiratory Distress Syndrome
Arterial Thrombosis Limb
Asthenia
Blood Alkaline Phosphatase Increased
Blood Pressure Decreased
Blood Pressure Systolic Increased
Bronchial Disorder
Cerebral Artery Stenosis
Difficulty In Walking
Disseminated Intravascular Coagulation
Drooling
Electrolyte Imbalance
FallWhat is Fall?
Gait Disturbance
Genital Haemorrhage
Hepatic Function Abnormal
Hypoaesthesia
Hypokalaemia
Hypoxia
Inadequate Analgesia
Insomnia
Liver Disorder
Myalgia
Oedema Peripheral
PainWhat is Pain?
Pain In Extremity
Platelet Count Decreased
Pleural Effusion
PneumoniaWhat is Pneumonia?
Pyrexia
Leuplin 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 Leuplin 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!