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Lopril adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 6. View All

Lopril FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 9

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

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5307586-3 | Dehydration, Hyponatraemia, Pyrexia
on Apr 23, 2007 Male patient from FRANCE , 78 years of age, was treated with Lopril (View Usage). Patient experienced the following unwanted or unexpected effects: dehydration, hyponatraemia, pyrexia. Lopril dosage: . During the same period patient was treated with GLUCOPHAGE (View Glucophage Review and Glucophage Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), TROPATEPINE (View Tropatepine Review and Tropatepine Label ). Patient was hospitalized.

5176885-0 | Alanine Aminotransferase Increased, Back Pain, Balance Disorder, Bronchitis, Confusional State, Cytolytic Hepatitis, Haemoptysis, Memory Impairment, Nervous System Disorder
Patient was taking Lopril (View Usage). Patient had the following side effects: alanine aminotransferase increased, back pain (What is back pain?), balance disorder, bronchitis (What is bronchitis?), confusional state, cytolytic hepatitis, haemoptysis, memory impairment, nervous system disorder on Dec 04, 2006 from FRANCE Additional patient health information: Female patient , 69 years of age, weighting 121.3 lb, . Lopril dosage: . During the same period patient was treated with TANAKAN (3 Df, Bid) (View Tanakan Review and Tanakan Label ), PROZAC (20 Mg, Qd) (View Prozac Review and Prozac Label ), LAMISIL (250 Mg, Qd) (View Lamisil Review and Lamisil Label ). Patient was hospitalized.

5082575-5 | Vascular Purpura
Adverse event was reported on Aug 07, 2006 by a Male patient taking Lopril (View Usage) (Dosage: ) . Location: FRANCE , 78 years of age, After Lopril was administered, patient had the following side effects: vascular purpura. During the same period patient was treated with LASILIX (View Lasilix Review and Lasilix Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), VASTAREL (View Vastarel Review and Vastarel Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

4621936-2 | Agranulocytosis, Laryngeal Dyspnoea, Leukopenia
on Jan 27, 2005 Female patient from , 40 years of age, weighting 134.5 lb, was diagnosed with essential hypertension, renal failure chronic, anaemia and was treated with Lopril (View Usage). Patient experienced the following unwanted or unexpected effects: agranulocytosis, laryngeal dyspnoea, leukopenia. Lopril dosage: . During the same period patient was treated with PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), LASILIX (View Lasilix Review and Lasilix Label ), PREVISCAN (View Previscan Review and Previscan Label ), ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), NEORECORMON (View Neorecormon Review and Neorecormon Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ), DOLIPRANE (View Doliprane Review and Doliprane Label ). Patient was hospitalized.


4611360-0 | Acute Respiratory Distress Syndrome, Bronchospasm, Cardiopulmonary Failure, Dysphagia
on Mar 07, 2005 Female patient from , 85 years of age, was diagnosed with hypertension, acute respiratory distress syndrome and was treated with Lopril (View Usage). Patient had the following side effects: acute respiratory distress syndrome, bronchospasm, cardiopulmonary failure, dysphagia. Lopril dosage: . During the same period patient was treated with ATROVENT (View Atrovent Review and Atrovent Label ), BRICANYL (View Bricanyl Review and Bricanyl Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), MONO TILDIEM (View Mono-tildiem Review and Mono-tildiem Label ), VASTAREL (View Vastarel Review and Vastarel Label ), SURBRONC (View Surbronc Review and Surbronc Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), DIAMICRON (View Diamicron Review and Diamicron Label ). Patient was hospitalized.

4591332-5 | Agranulocytosis, Laryngeal Dyspnoea
Patient was taking Lopril (View Usage). After Lopril was administered, patient had the following side effects: agranulocytosis, laryngeal dyspnoea on Jan 27, 2005 from Additional patient health information: Female patient , 40 years of age, weighting 134.5 lb, was diagnosed with hypertension, renal failure chronic and. Lopril dosage: . During the same period patient was treated with PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), LASILIX (View Lasilix Review and Lasilix Label ), PREVISCAN (View Previscan Review and Previscan Label ), STILNOX (View Stilnox Review and Stilnox Label ), NEORECORMON (View Neorecormon Review and Neorecormon Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ), DOLIPRANE (View Doliprane Review and Doliprane Label ). Patient was hospitalized.


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Lopril Questions, Answers, Feedback and Comments

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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 Lopril 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 Lopril quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lopril 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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During the same period patient was treated with LOPRIL (View Lopril Review and Lopril Label ), WYSOLONE (5 Mg, Unk) (View Wysolone Review and Wysolone Label ), XANTINOL ...

During the same period patient was treated with LOPRIL (View Lopril Review and Lopril Label ), WYSOLONE (5 Mg, Unk) (View Wysolone Review and Wysolone Label ), XANTINOL ...

Crestor Review and Crestor Label ), LASILIX (View Lasilix Review and Lasilix Label ), LOPRIL (View Lopril Review and Lopril Label ), TARDYFERON (View Tardyferon Review and ...

... same period patient was treated with GLUCOPHAGE (View Glucophage Review and Glucophage Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), LOPRIL ...

... Zyloric Review and Zyloric Label ), CRESTOR (View Crestor Review and Crestor Label ), LASILIX (View Lasilix Review and Lasilix Label ), LOPRIL (View Lopril Review and Lopril ...

During the same period patient was treated with LOPRIL (View Lopril Review and Lopril Label ). Patient was hospitalized. 4959614-2 | Anaemia, Thrombocytopenic Purpura

During the same period patient was treated with LOPRIL (View Lopril Review and Lopril Label ), ALDALIX (View Aldalix Review and Aldalix Label ), LEXOMIL (View Lexomil Review ...

During the same period patient was treated with ADALAT (20mg Per Day) (View Adalat Review and Adalat Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), LOPRIL ...

... Adalat Review and Adalat Label ), LOPRIL /00498401/ (View Lopril /00498401/ Review and Lopril ...

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Lopril Reactions
Acute Respiratory Distress Syndrome
Agranulocytosis
Alanine Aminotransferase Increased
Back PainWhat is Back pain?
Balance Disorder
BronchitisWhat is Bronchitis?
Bronchospasm
Cardiopulmonary Failure
Confusional State
Cytolytic Hepatitis
Dehydration
Dysphagia
Haemoptysis
Hyponatraemia
Laryngeal Dyspnoea
Leukopenia
Memory Impairment
Nervous System Disorder
Pyrexia
Vascular Purpura
Lopril 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 Lopril 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!