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Little Increase In Heart Beat (7)
My Mouth Became Dri (6)
Tachycardia (6)
Indication Of Salbutamol (5)
Cataract (2)
Change Inmentral Cycle (2)
Flammable Skin Irritation Especially The Face (2)
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Common Salbutamol Side Effects

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Salbutamol adverse events reported to FDA.

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Summary

FDA Adverse Reports: 73. View All

Salbutamol FDA safety alerts: No

Reported deaths: 13

Reported hospitalizations: 23

More About Salbutamol

Post Your Unusual Symptoms:

Most Reported
1Tachycardia
2Indication Of Salbutamol
3Little Increase In Heart Beat
4My Mouth Became Dri
5Irregular Tiredness
6Flammable Skin Irritation Especially The Face
7Cataract
8Saw Teeth Bulbs Walls Larger After Taking The Dosa
9Little Increase In Heart Beat, My Mouth Became Dri
10Change Inmentral Cycle
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Often additional risks of using a medication, such as Salbutamol, 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 Salbutamol users, Learn more about unwanted side effects & find ways to reduce them. Browse Salbutamol Adverse Reports reported to FDA and participate in Salbutamol discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Salbutamol. 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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Salbutamol Adverse Effect Reports (FDA)

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6836716-7 | Lactic Acidosis
on Jun 29, 2010 Female patient from UNITED STATES , 44 years of age, was diagnosed with asthma (What is asthma?), stridor and was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: lactic acidosis. Salbutamol dosage: . During the same period patient was treated with SALMETEROL (1 Prolonged Course) (View Salmeterol Review and Salmeterol Label ), EPINEPHRINE (View Epinephrine Review and Epinephrine Label ). Patient was hospitalized.

6836713-1 | Lactic Acidosis
Patient was taking Salbutamol (View Usage). Patient had the following side effects: lactic acidosis on Jun 29, 2010 from UNITED STATES Additional patient health information: Male patient , 32 years of age, was diagnosed with asthma (What is asthma?), respiratory failure and. Salbutamol dosage: . Patient was hospitalized.

6747203-9 | Hyperlactacidaemia
Adverse event was reported on May 13, 2010 by a Female patient taking Salbutamol (View Usage) (Dosage: ) was diagnosed with asthma (What is asthma?) and. Location: GERMANY , 17 years of age, After Salbutamol was administered, patient had the following side effects: hyperlactacidaemia. During the same period patient was treated with THEOPHYLLINE (View Theophylline Review and Theophylline Label ), BUDESONIDE (View Budesonide Review and Budesonide Label ), FORMOTEROL (View Formoterol Review and Formoterol Label ), MONTELUKAST SODIUM (View Montelukast Sodium Review and Montelukast Sodium Label ).

6741382-5 | Hellp Syndrome, Left Atrial Dilatation, Mitral Valve Incompetence, Mitral Valve Stenosis, Pre-eclampsia, Pulmonary Hypertension, Pulmonary Oedema
on May 14, 2010 Female patient from UNITED KINGDOM , 32 years of age, was diagnosed with wheezing, tachycardia and was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: hellp syndrome, left atrial dilatation, mitral valve incompetence, mitral valve stenosis, pre-eclampsia, pulmonary hypertension (What is pulmonary hypertension?), pulmonary oedema. Salbutamol dosage: Started At 14 Weeks Gestation. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), FRUSEMIDE (View Frusemide Review and Frusemide Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), ENOXAPARIN SODIUM (View Enoxaparin Sodium Review and Enoxaparin Sodium Label ), METOPROLOL (Total Daily Dose: 25 Mg) (View Metoprolol Review and Metoprolol Label ), FLUIDS (View Fluids Review and Fluids Label ).


6724064-5 | Myalgia
on May 05, 2010 Male patient from UNITED STATES , 64 years of age, was treated with Salbutamol (View Usage). Patient had the following side effects: myalgia. Salbutamol dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), PROCATEROL HCL (View Procaterol Hcl Review and Procaterol Hcl Label ).

6711774-9 | Asthma, Condition Aggravated, Cough, Dyspnoea, Foreign Body Aspiration, Rales, Wheezing
Patient was taking Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: asthma (What is asthma?), condition aggravated, cough, dyspnoea, foreign body aspiration, rales, wheezing on Apr 23, 2010 from MOROCCO Additional patient health information: Female patient , 22 years of age, was diagnosed with asthma (What is asthma?) and. Salbutamol dosage: .

6698982-0 | Dizziness, Hypotension, Malaise, Nausea, Stress Cardiomyopathy, Tachycardia
Adverse event was reported on Apr 19, 2010 by a Female patient taking Salbutamol (View Usage) (Dosage: ) . Location: GERMANY , 51 years of age, weighting 143.3 lb, Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), hypotension, malaise, nausea (What is nausea?), stress cardiomyopathy, tachycardia. During the same period patient was treated with THEOPHYLLINE SR (375mg Twice Per Day) (View Theophylline-sr Review and Theophylline-sr Label ), SPIRIVA (18mcg Per Day) (View Spiriva Review and Spiriva Label ), SYMBICORT (329mcg Twice Per Day) (View Symbicort Review and Symbicort Label ), RAMIPRIL (2.5mg Twice Per Day) (View Ramipril Review and Ramipril Label ). Patient was hospitalized.

6690608-5 | Dermatitis Allergic, Pruritus, Restlessness
on Apr 12, 2010 Female patient from GERMANY , 36 years of age, weighting 143.3 lb, was diagnosed with respiratory tract infection, immunodeficiency and was treated with Salbutamol (View Usage). Patient had the following side effects: dermatitis allergic, pruritus, restlessness. Salbutamol dosage: . During the same period patient was treated with CLINDAMYCIN HCL (600mg Twice Per Day) (View Clindamycin Hcl Review and Clindamycin Hcl Label ), VIVAGLOBIN (20ml Per Day) (View Vivaglobin Review and Vivaglobin Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), AMPICILLIN AND SULBACTAM (375mg Twice Per Day) (View Ampicillin And Sulbactam Review and Ampicillin And Sulbactam Label ), RULID (300mg Per Day) (View Rulid Review and Rulid Label ). Patient was hospitalized.

6664158-6 | Aortic Valve Disease, Atrial Fibrillation, Heart Rate Increased
on Mar 25, 2010 Female patient from UNITED STATES , 71 years of age, was diagnosed with wheezing and was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: aortic valve disease, atrial fibrillation (What is atrial fibrillation?), heart rate increased. Salbutamol dosage: 2puff Four Times Per Day. During the same period patient was treated with PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), IRBESARTAN (View Irbesartan Review and Irbesartan Label ), CIPROFLOXACIN (View Ciprofloxacin Review and Ciprofloxacin Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), MONTELUKAST SODIUM (View Montelukast Sodium Review and Montelukast Sodium Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), BUDESONIDE (View Budesonide Review and Budesonide Label ). Patient was hospitalized.

6664129-X | Asthma, Overdose
Patient was taking Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: asthma (What is asthma?), overdose on Mar 24, 2010 from UNITED KINGDOM Additional patient health information: Female patient , child 10 years of age, was diagnosed with asthma (What is asthma?) and. Salbutamol dosage: 6u Per Day. During the same period patient was treated with SERETIDE (4u Per Day) (View Seretide Review and Seretide Label ).

6658174-8 | Asthma, Overdose
Adverse event was reported on Mar 23, 2010 by a Female patient taking Salbutamol (View Usage) (Dosage: 6u Per Day) was diagnosed with asthma (What is asthma?) and. Location: UNITED KINGDOM , child 10 years of age, Patient had the following side effects: asthma (What is asthma?), overdose. During the same period patient was treated with SERETIDE (4u Per Day) (View Seretide Review and Seretide Label ).

6367401-6 | Asthma, Product Quality Issue
on Sep 16, 2009 Female patient from CANADA , 63 years of age, was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: asthma (What is asthma?), product quality issue. Salbutamol dosage: 2puff Four Times Per Day. Patient was hospitalized.

6359855-6 | Chronic Obstructive Pulmonary Disease
on Sep 05, 2009 Male patient from UNITED KINGDOM , 93 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: chronic obstructive pulmonary disease. Salbutamol dosage: . During the same period patient was treated with ATROVENT (View Atrovent Review and Atrovent Label ).

6359821-0 | Asthma, Product Quality Issue
Patient was taking Salbutamol (View Usage). Patient had the following side effects: asthma (What is asthma?), product quality issue on Sep 16, 2009 from CANADA Additional patient health information: Female patient , 63 years of age, . Salbutamol dosage: 2puff Four Times Per Day. Patient was hospitalized.

6337482-4 | Chronic Obstructive Pulmonary Disease
Adverse event was reported on Aug 26, 2009 by a Male patient taking Salbutamol (View Usage) (Dosage: ) was diagnosed with chronic obstructive pulmonary disease and. Location: UNITED KINGDOM , 93 years of age, After Salbutamol was administered, patient had the following side effects: chronic obstructive pulmonary disease. During the same period patient was treated with IPRATROPIUM BROMIDE (View Ipratropium Bromide Review and Ipratropium Bromide Label ).

6316398-3 | Asthma
on Aug 14, 2009 Female patient from UNITED KINGDOM , 33 years of age, was diagnosed with toothache and was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: asthma (What is asthma?). Salbutamol dosage: . During the same period patient was treated with METHADONE (View Methadone Review and Methadone Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), FLUTICASONE (View Fluticasone Review and Fluticasone Label ), NICOTINE (View Nicotine Review and Nicotine Label ). Patient was hospitalized.

6311645-6 | Chest Discomfort, Ear Pain, Palpitations
on Aug 07, 2009 Female patient from UNITED KINGDOM , 65 years of age, was diagnosed with breast cancer (What is breast cancer?) and was treated with Salbutamol (View Usage). Patient had the following side effects: chest discomfort, ear pain, palpitations. Salbutamol dosage: . During the same period patient was treated with ANASTROZOLE (1mg Per Day) (View Anastrozole Review and Anastrozole Label ), OMEPRAZOLE (20mg Per Day) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6199588-2 | Blood Potassium Decreased, Blood Sodium Decreased, Metabolic Alkalosis
Patient was taking Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: blood potassium decreased, blood sodium decreased, metabolic alkalosis on May 13, 2009 from GERMANY Additional patient health information: Female patient , 51 years of age, weighting 202.8 lb, was diagnosed with cardiac failure, hypereosinophilic syndrome and. Salbutamol dosage: . During the same period patient was treated with XIPAMIDE (20mg Per Day) (View Xipamide Review and Xipamide Label ), TORSEMIDE (View Torsemide Review and Torsemide Label ), PREDNISOLONE (30mg Per Day) (View Prednisolone Review and Prednisolone Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), COLECALCIFEROL (View Colecalciferol Review and Colecalciferol Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ). Patient was hospitalized.

6197972-4 | Cough, Diarrhoea, Dizziness, Dyspnoea, Hypokalaemia, Hyponatraemia, Metabolic Alkalosis
Adverse event was reported on May 18, 2009 by a Female patient taking Salbutamol (View Usage) (Dosage: ) was diagnosed with hypereosinophilic syndrome, renal osteodystrophy and. Location: GERMANY , 51 years of age, weighting 202.8 lb, Patient experienced the following unwanted or unexpected effects: cough, diarrhoea, dizziness (What is dizziness?), dyspnoea, hypokalaemia, hyponatraemia, metabolic alkalosis. During the same period patient was treated with AQUAPHOR (20mg Per Day) (View Aquaphor Review and Aquaphor Label ), TORSEMIDE (120mg Per Day) (View Torsemide Review and Torsemide Label ), ALDACTONE (50mg Twice Per Day) (View Aldactone Review and Aldactone Label ), PREDNISOLONE (100mg Per Day) (View Prednisolone Review and Prednisolone Label ), ASPIRIN (100mg Per Day) (View Aspirin Review and Aspirin Label ), BISOPROLOL (2.5mg Per Day) (View Bisoprolol Review and Bisoprolol Label ), CALCILAC (500mg Per Day) (View Calcilac Review and Calcilac Label ), FALITHROM (3mg Single Dose) (View Falithrom Review and Falithrom Label ). Patient was hospitalized.

6179205-8 | Acute Myocardial Infarction, Chest Pain, Throat Irritation
on Apr 28, 2009 Female patient from UNITED KINGDOM , 78 years of age, weighting 165.3 lb, was diagnosed with asthma (What is asthma?), type 2 diabetes mellitus, colon cancer and was treated with Salbutamol (View Usage). Patient had the following side effects: acute myocardial infarction, chest pain (What is chest pain?), throat irritation. Salbutamol dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), OXALIPLATIN (View Oxaliplatin Review and Oxaliplatin Label ). Patient was hospitalized.

6160256-4 | Enamel Anomaly, Loose Tooth
on Apr 13, 2009 Male patient from NETHERLANDS , weighting 114.6 lb, was diagnosed with asthma (What is asthma?) and was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: enamel anomaly, loose tooth. Salbutamol dosage: . During the same period patient was treated with BUDESONIDE (View Budesonide Review and Budesonide Label ), MONTELUKAST (10mg Per Day) (View Montelukast Review and Montelukast Label ).

6159263-7 | Enamel Anomaly, Tooth Disorder
Patient was taking Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: enamel anomaly, tooth disorder (What is tooth disorder?) on Apr 07, 2009 from NETHERLANDS Additional patient health information: Male patient , weighting 114.6 lb, was diagnosed with asthma (What is asthma?) and. Salbutamol dosage: . During the same period patient was treated with BUDESONIDE (View Budesonide Review and Budesonide Label ), MONTELUKAST (View Montelukast Review and Montelukast Label ).

6144733-8 | Emphysema, Increased Upper Airway Secretion, Pneumonia
Adverse event was reported on Apr 02, 2009 by a Female patient taking Salbutamol (View Usage) (Dosage: ) was diagnosed with chronic obstructive pulmonary disease and. Location: UNITED KINGDOM , 71 years of age, weighting 130.1 lb, Patient had the following side effects: emphysema, increased upper airway secretion, pneumonia (What is pneumonia?). During the same period patient was treated with IPRATROPIUM BROMIDE (View Ipratropium Bromide Review and Ipratropium Bromide Label ), SERETIDE (2 Df B.i.d) (View Seretide Review and Seretide Label ). Patient was hospitalized and became disabled.

6144699-0 | Swelling Face
on Mar 30, 2009 Female patient from UNITED KINGDOM , 45 years of age, was diagnosed with asthma (What is asthma?) and was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: swelling face. Salbutamol dosage: . During the same period patient was treated with CLENIL MODULITE (View Clenil Modulite Review and Clenil Modulite Label ).

6139895-2 | Thermal Burn
on Mar 23, 2009 Male patient from UNITED KINGDOM , 13 years of age, was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: thermal burn. Salbutamol dosage: . Patient was hospitalized.

6126948-8 | Thermal Burn
Patient was taking Salbutamol (View Usage). Patient had the following side effects: thermal burn on Mar 09, 2009 from UNITED KINGDOM Additional patient health information: Male patient , 13 years of age, . Salbutamol dosage: . Patient was hospitalized.

5867038-9 | Apgar Score Low, Caesarean Section, Foetal Distress Syndrome, Neonatal Respiratory Failure, Premature Baby, Respiratory Disorder, Tachycardia Foetal
Adverse event was reported on Aug 21, 2008 by a Male patient taking Salbutamol (View Usage) (Dosage: ) was diagnosed with asthma (What is asthma?) and. Location: UNITED KINGDOM , weighting 7.72 lb, After Salbutamol was administered, patient had the following side effects: apgar score low, caesarean section, foetal distress syndrome, neonatal respiratory failure, premature baby, respiratory disorder, tachycardia foetal. During the same period patient was treated with AMINOPHYLLINE (View Aminophylline Review and Aminophylline Label ), ATROVENT (View Atrovent Review and Atrovent Label ), OXYGEN (View Oxygen Review and Oxygen Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), SALMETEROL (View Salmeterol Review and Salmeterol Label ).

5725858-5 |
on Apr 14, 2008 Male patient from UNITED STATES , 65 years of age, was treated with Salbutamol (View Usage). . Salbutamol dosage: . During the same period patient was treated with RISPERIDONE (View Risperidone Review and Risperidone Label ), METAXALONE (View Metaxalone Review and Metaxalone Label ), HEPARIN (View Heparin Review and Heparin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ESCITALOPRAM (View Escitalopram Review and Escitalopram Label ), BUPROPION HCL (View Bupropion Hcl Review and Bupropion Hcl Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label ).

5725714-2 |
on Apr 14, 2008 Male patient from UNITED KINGDOM , 65 years of age, was treated with Salbutamol (View Usage). . Salbutamol dosage: . During the same period patient was treated with RISPERIDONE (View Risperidone Review and Risperidone Label ), METAXALONE (View Metaxalone Review and Metaxalone Label ), HEPARIN (View Heparin Review and Heparin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ESCITALOPRAM (View Escitalopram Review and Escitalopram Label ), BUPROPION HCL (View Bupropion Hcl Review and Bupropion Hcl Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label ).

5700886-4 | Abnormal Faeces, Dysgeusia, Urine Odour Abnormal
Patient was taking Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: abnormal faeces, dysgeusia, urine odour abnormal on Apr 02, 2008 from CANADA Additional patient health information: Female patient , 63 years of age, was diagnosed with asthma (What is asthma?) and. Salbutamol dosage: 2puff Per Day. During the same period patient was treated with PULMICORT (View Pulmicort Review and Pulmicort Label ).

5700804-9 | Thermal Burn
Adverse event was reported on Apr 02, 2008 by a Male patient taking Salbutamol (View Usage) (Dosage: ) . Location: UNITED KINGDOM , child 11 years of age, Patient experienced the following unwanted or unexpected effects: thermal burn.

5683413-X |
on Mar 11, 2008 Male patient from UNITED STATES , 65 years of age, was treated with Salbutamol (View Usage). . Salbutamol dosage: .

5683411-6 | Completed Suicide
on Mar 11, 2008 Female patient from UNITED STATES , 43 years of age, was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: completed suicide. Salbutamol dosage: .

5683396-2 | Glycosuria, Metabolic Acidosis, Respiratory Distress, Tachypnoea
Patient was taking Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: glycosuria, metabolic acidosis, respiratory distress, tachypnoea on Mar 11, 2008 from UNITED STATES Additional patient health information: Male patient , child 6 years of age, . Salbutamol dosage: 2.5 Mg; Every 4 Hours.

5683382-2 | Metabolic Acidosis, Respiratory Acidosis, Tachypnoea
Adverse event was reported on Mar 11, 2008 by a Male patient taking Salbutamol (View Usage) (Dosage: 15 Mg/hr) . Location: UNITED STATES , child 12 years of age, Patient had the following side effects: metabolic acidosis, respiratory acidosis, tachypnoea.

5683379-2 | Glycosuria, Hypotension, Metabolic Acidosis, Tachycardia, Tachypnoea
on Mar 11, 2008 Male patient from UNITED STATES , 17 years of age, was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: glycosuria, hypotension, metabolic acidosis, tachycardia, tachypnoea. Salbutamol dosage: 2.5mg; 15 Mh;hr.

5683375-5 | Asthma, Choking Sensation, Foreign Body Aspiration, Obstructive Airways Disorder, Pneumomediastinum, Pneumothorax, Wheezing
on Mar 11, 2008 Male patient from UNITED STATES , 43 years of age, was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: asthma (What is asthma?), choking sensation, foreign body aspiration, obstructive airways disorder, pneumomediastinum, pneumothorax, wheezing. Salbutamol dosage: .

5683370-6 | Blood Pressure Decreased, Condition Aggravated, Hyperglycaemia, Metabolic Acidosis, Mucosal Dryness, Polyuria, Somnolence
Patient was taking Salbutamol (View Usage). Patient had the following side effects: blood pressure decreased, condition aggravated, hyperglycaemia, metabolic acidosis, mucosal dryness, polyuria, somnolence on Mar 11, 2008 from UNITED STATES Additional patient health information: Female patient , child 8 years of age, . Salbutamol dosage: 0.5 Mg/kg.

5683368-8 | Apnoea, Bronchospasm Paradoxical, Chest Discomfort, Influenza Like Illness, Loss Of Consciousness
Adverse event was reported on Mar 11, 2008 by a Male patient taking Salbutamol (View Usage) (Dosage: ) . Location: UNITED STATES , 59 years of age, After Salbutamol was administered, patient had the following side effects: apnoea, bronchospasm paradoxical, chest discomfort, influenza like illness, loss of consciousness.

5444383-2 | Atrial Fibrillation, Electrocardiogram Qrs Complex Shortened, No Therapeutic Response, Tachycardia
on Oct 02, 2006 Female patient from UNITED KINGDOM , 76 years of age, weighting 88.18 lb, was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: atrial fibrillation (What is atrial fibrillation?), electrocardiogram qrs complex shortened, no therapeutic response, tachycardia. Salbutamol dosage: Inh. During the same period patient was treated with THEOPHYLLINE (200 Mg 1/d Po) (View Theophylline Review and Theophylline Label ), BUDESONIDE (View Budesonide Review and Budesonide Label ), CARBOCYSTEINE (View Carbocysteine Review and Carbocysteine Label ), CO CODAMOL (View Co-codamol Review and Co-codamol Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), IPRATROPIUM BROMIDE (View Ipratropium Bromide Review and Ipratropium Bromide Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.

5400411-1 | Apgar Score Low, Foetal Distress Syndrome, Premature Baby, Tachycardia Foetal
on Jul 17, 2007 Male patient from UNITED KINGDOM , weighting 7.72 lb, was diagnosed with asthma (What is asthma?) and was treated with Salbutamol (View Usage). Patient had the following side effects: apgar score low, foetal distress syndrome, premature baby, tachycardia foetal. Salbutamol dosage: . During the same period patient was treated with AMINOPHYLLINE (View Aminophylline Review and Aminophylline Label ), ATROVENT (View Atrovent Review and Atrovent Label ), OXYGEN (View Oxygen Review and Oxygen Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), SALMETEROL (View Salmeterol Review and Salmeterol Label ).

5399277-8 | Apgar Score Low, Foetal Distress Syndrome, Premature Baby, Tachycardia Foetal
Patient was taking Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: apgar score low, foetal distress syndrome, premature baby, tachycardia foetal on Jul 17, 2007 from UNITED KINGDOM Additional patient health information: Male patient , weighting 7.72 lb, was diagnosed with asthma (What is asthma?) and. Salbutamol dosage: . During the same period patient was treated with AMINOPHYLLINE (View Aminophylline Review and Aminophylline Label ), ATROVENT (View Atrovent Review and Atrovent Label ), OXYGEN (View Oxygen Review and Oxygen Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), SALMETEROL (View Salmeterol Review and Salmeterol Label ).

5399276-6 | Asthma, Dehydration, Dyspnoea, Hyperventilation, Lung Hyperinflation, Metabolic Acidosis, Operative Haemorrhage, Oral Intake Reduced, Peak Expiratory Flow Rate Increased
Adverse event was reported on Jul 17, 2007 by a Female patient taking Salbutamol (View Usage) (Dosage: ) was diagnosed with asthma (What is asthma?) and. Location: UNITED KINGDOM , 31 years of age, Patient experienced the following unwanted or unexpected effects: asthma (What is asthma?), dehydration, dyspnoea, hyperventilation, lung hyperinflation, metabolic acidosis, operative haemorrhage, oral intake reduced, peak expiratory flow rate increased. During the same period patient was treated with AMINOPHYLLINE (View Aminophylline Review and Aminophylline Label ), ATROVENT (View Atrovent Review and Atrovent Label ), OXYGEN (View Oxygen Review and Oxygen Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), SALMETEROL (View Salmeterol Review and Salmeterol Label ).

5380574-7 | Abdominal Pain, Abdominal Rigidity, Blood Ph Increased, Carbon Dioxide Increased, Hyperlactacidaemia
on Jun 20, 2007 Female patient from UNITED KINGDOM , 28 years of age, was diagnosed with asthma (What is asthma?) and was treated with Salbutamol (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), abdominal rigidity, blood ph increased, carbon dioxide increased, hyperlactacidaemia. Salbutamol dosage: 5 Mg. Patient was hospitalized.

5330020-4 | Asthma
on May 11, 2007 Female patient from UNITED KINGDOM , 36 years of age, was diagnosed with asthma (What is asthma?) and was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: asthma (What is asthma?). Salbutamol dosage: . During the same period patient was treated with LACTULOSE (View Lactulose Review and Lactulose Label ), SERETIDE (View Seretide Review and Seretide Label ), VENTOLIN (View Ventolin Review and Ventolin Label ), STEROID (View Steroid Review and Steroid Label ).

5296230-X | Caesarean Section, Gestational Diabetes, Premature Baby, Premature Rupture Of Membranes
Patient was taking Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, gestational diabetes, premature baby, premature rupture of membranes on Apr 03, 2007 from GREECE Additional patient health information: Female patient , 23 years of age, was diagnosed with tocolysis, infection prophylaxis, gestational diabetes and. Salbutamol dosage: 4mg Three Times Per Day. During the same period patient was treated with AMOXICILLIN + CLAVULANIC ACID (View Amoxicillin + Clavulanic Acid Review and Amoxicillin + Clavulanic Acid Label ), TICARCILLIN + CLAVULANIC ACID (3.2mg Three Times Per Day) (View Ticarcillin + Clavulanic Acid Review and Ticarcillin + Clavulanic Acid Label ), BETAMETHASONE (12mg See Dosage Text) (View Betamethasone Review and Betamethasone Label ), METRONIDAZOLE (500mg Three Times Per Day) (View Metronidazole Review and Metronidazole Label ), ENOXAPARIN SODIUM (40mg Per Day) (View Enoxaparin Sodium Review and Enoxaparin Sodium Label ), INSULIN (View Insulin Review and Insulin Label ).

5128571-0 | Agitation, Dyspnoea, Hyperglycaemia, Hyperhidrosis, Hypokalaemia, Hypotension, Mydriasis, Sinus Tachycardia
Adverse event was reported on Sep 21, 2006 by a Female patient taking Salbutamol (View Usage) (Dosage: 300mg Single Dose) . Location: ISRAEL , 20 years of age, Patient had the following side effects: agitation, dyspnoea, hyperglycaemia, hyperhidrosis, hypokalaemia, hypotension, mydriasis, sinus tachycardia. During the same period patient was treated with ACETAMINOPHEN (30g Single Dose) (View Acetaminophen Review and Acetaminophen Label ).

5123288-0 | Blood Glucose Increased, Diabetic Ketoacidosis, Ketonuria, Normal Delivery, Premature Labour
on Oct 02, 2006 Female patient from UNITED KINGDOM , 26 years of age, was treated with Salbutamol (View Usage). After Salbutamol was administered, patient had the following side effects: blood glucose increased, diabetic ketoacidosis, ketonuria, normal delivery, premature labour. Salbutamol dosage: . During the same period patient was treated with INSULIN (View Insulin Review and Insulin Label ), GLUCOSE (View Glucose Review and Glucose Label ).

5123287-9 | Blood Glucose Increased, Diabetic Ketoacidosis, Ketonuria, Somnolence
on Oct 02, 2006 Female patient from UNITED KINGDOM , 24 years of age, was treated with Salbutamol (View Usage). Patient experienced the following unwanted or unexpected effects: blood glucose increased, diabetic ketoacidosis, ketonuria, somnolence. Salbutamol dosage: .

5123286-7 | Glycosuria, Hyperglycaemia, Ketoacidosis, Ketosis
Patient was taking Salbutamol (View Usage). Patient had the following side effects: glycosuria, hyperglycaemia, ketoacidosis, ketosis on Oct 02, 2006 from UNITED KINGDOM Additional patient health information: Female patient , 45 years of age, was diagnosed with asthma (What is asthma?) and. Salbutamol dosage: . During the same period patient was treated with PREDNISONE (15mg See Dosage Text) (View Prednisone Review and Prednisone Label ), FLUIDS (View Fluids Review and Fluids Label ), OXYGEN (View Oxygen Review and Oxygen Label ), HYDROCORTISONE (500mg See Dosage Text) (View Hydrocortisone Review and Hydrocortisone Label ), AMINOPHYLLINE (View Aminophylline Review and Aminophylline Label ).

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Salbutamol Questions, Answers, Feedback and Comments

Comments to date: 4. Page 1 of 1.

sosina   Amarat

3:19pm on Friday, October 23rd, 2009

Is salbutamol loss the weight and appetite?

kavita   ajmer

2:49pm on Saturday, September 5th, 2009

effect of salbutamol on liver functions

ghazi zbeeb   Qatar

11:55pm on Friday, August 14th, 2009

does Salbutamol increase weight ?

drina de pineda   guatemala ciudad zona 14

3:10pm on Wednesday, August 5th, 2009

my baby of 4 months is

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 Salbutamol 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 Salbutamol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Salbutamol 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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Salbutamol Reactions
Acute Myocardial Infarction
Agitation
Amnesia
Apgar Score Low
Apnoea
AsthmaWhat is Asthma?
Blood Glucose Increased
Bronchospasm
Bronchospasm Paradoxical
Chronic Obstructive Pulmonary Disease
Cough
Death
Diabetic Ketoacidosis
Dyspnoea
Emphysema
Foetal Distress Syndrome
Glycosuria
Hyperglycaemia
Hypokalaemia
Hypotension
Lactic Acidosis
Metabolic Acidosis
Mydriasis
Oxygen Saturation Decreased
Premature Baby
Respiratory Acidosis
Tachycardia
Tachycardia Foetal
Tachypnoea
Thermal Burn
Salbutamol 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 Salbutamol 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!