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Summary

FDA Adverse Reports: 131. View All

Betamethasone FDA safety alerts: No

Reported deaths: 16

Reported hospitalizations: 84

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

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6771152-3 | Burning Sensation, Pain, Pruritus
on Jun 14, 2010 Female patient from UNITED STATES , weighting 120.0 lb, was diagnosed with eczema (What is eczema?), pruritus and was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: burning sensation, pain (What is pain?), pruritus. Betamethasone dosage: Ndc 0136-0041-60.

6743475-5 | Microscopic Polyangiitis
Patient was taking Betamethasone (View Usage). Patient had the following side effects: microscopic polyangiitis on Nov 06, 2009 from UNITED KINGDOM Additional patient health information: Female patient , weighting 3.17 lb, was diagnosed with pregnancy (What is pregnancy?) and. Betamethasone dosage: Trpl. During the same period patient was treated with PREDNISOLONE (Trpl) (View Prednisolone Review and Prednisolone Label ), METHYLPREDNISOLONE (Trpl) (View Methylprednisolone Review and Methylprednisolone Label ), CYCLOPHOSPHAMIDE (Trpl) (View Cyclophosphamide Review and Cyclophosphamide Label ), TRIMETHOPRIM + SULFAMETHOXAZOLE (Trpl) (View Trimethoprim + Sulfamethoxazole Review and Trimethoprim + Sulfamethoxazole Label ).

6742838-1 | Abnormal Behaviour, Circulatory Collapse, Coagulopathy, Cold Sweat, Fall, Haemorrhagic Stroke, Hypertension, Initial Insomnia
Adverse event was reported on Nov 06, 2009 by a Male patient taking Betamethasone (View Usage) (Dosage: 50 Mg;prn;top) was diagnosed with neuropathy peripheral, blood pressure (What is blood pressure?), pain (What is pain?), insomnia, micturition disorder, diabetes mellitus and. Location: UNITED STATES , 72 years of age, weighting 299.9 lb, After Betamethasone was administered, patient had the following side effects: abnormal behaviour, circulatory collapse, coagulopathy, cold sweat, fall (What is fall?), haemorrhagic stroke, hypertension, initial insomnia. During the same period patient was treated with FENTANYL (50 Mcg; Tder) (View Fentanyl Review and Fentanyl Label ), METOPROLOL TARTRATE (50 Mg;bid;po) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), HYDROCODONE BITARTRATE + ACETAMINOPHEN (6 Df;qd;po) (View Hydrocodone Bitartrate + Acetaminophen Review and Hydrocodone Bitartrate + Acetaminophen Label ), AMBIEN (10 Mg;prn;po) (View Ambien Review and Ambien Label ), AMMONIUM LACTATE (400 Mg;bid;top) (View Ammonium Lactate Review and Ammonium Lactate Label ), UROXATRAL (10 Mg;qd;po) (View Uroxatral Review and Uroxatral Label ), OXYCONTIN (40 Mg;prn;po) (View Oxycontin Review and Oxycontin Label ), LANTUS (25 Gm;qd;sc) (View Lantus Review and Lantus Label ). Patient was hospitalized.

6540299-9 | Premature Labour, Premature Rupture Of Membranes
on Oct 27, 2009 Female patient from UNITED KINGDOM , 25 years of age, was diagnosed with microscopic polyangiitis, prophylaxis and was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: premature labour, premature rupture of membranes. Betamethasone dosage: (12 Mg, Two 12 Mg Intramuscular). During the same period patient was treated with PREDNISOLONE ((60 Mg, Dose Freq.: Daily Oral) ; 10 Mg, Maintenance Dose Dose Freq.: Daily Oral)) (View Prednisolone Review and Prednisolone Label ), METHYLPREDNISOLONE ((1 G, Dose Freq.: Daily Intravenous (not Otherwise Specified))) (View Methylprednisolone Review and Methylprednisolone Label ), CYCLOPHOSPHAMIDE (See Image) (View Cyclophosphamide Review and Cyclophosphamide Label ), TRIMETHOPRIM + SULFAMETHOXAZOLE (View Trimethoprim + Sulfamethoxazole Review and Trimethoprim + Sulfamethoxazole Label ), INSULIN (View Insulin Review and Insulin Label ). Patient was hospitalized.


6540209-4 | Kidney Malformation, Premature Baby
on Oct 27, 2009 Female patient from UNITED KINGDOM , weighting 3.09 lb, was diagnosed with microscopic polyangiitis, prophylaxis and was treated with Betamethasone (View Usage). Patient had the following side effects: kidney malformation, premature baby. Betamethasone dosage: (12 Mg, Two 12 Mg Transplacental). During the same period patient was treated with PREDNISOLONE ((60 Mg, Dose Freq: Daily Transplantal) ; (10 Mg, Maintenance Dose Dose Freq: Daily Oral)) (View Prednisolone Review and Prednisolone Label ), CYCLOPHOSPHAMIDE ((1 G, Dose Freq: Daily Transplacental)) (View Cyclophosphamide Review and Cyclophosphamide Label ), METHYLPREDNISOLONE ((1 G, Dose Freq.: Daily Transplacental)) (View Methylprednisolone Review and Methylprednisolone Label ), CO TRIMOXAZOEL (CO TRIMOXAZOLE) ((transplacental) A Few Weeks) (View Co-trimoxazoel (co-trimoxazole) Review and Co-trimoxazoel (co-trimoxazole) Label ), INSULIN (View Insulin Review and Insulin Label ). Patient was hospitalized.

6538521-8 | Premature Baby, Solitary Kidney, Ventouse Extraction
Patient was taking Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: premature baby, solitary kidney, ventouse extraction on Oct 27, 2009 from UNITED KINGDOM Additional patient health information: Female patient , weighting 3.09 lb, was diagnosed with microscopic polyangiitis, prophylaxis and. Betamethasone dosage: (12 Mg, Two 12 Mg Transplacental). During the same period patient was treated with PREDNISOLONE ((60 Mg, Dose Freq.: Daily Transplacental), (10 Mg, Maintenance Dose Dose Freq.: Daily Oral)) (View Prednisolone Review and Prednisolone Label ), CYCLOPHOSPHAMIDE ((1 G, Dose Freq.: Daily Transplacental) (1 G, Two 1 G Pulses Dose Freq.: Daily Intravenous))) (View Cyclophosphamide Review and Cyclophosphamide Label ), METHYLPREDNISOLONE ((1 G, Dose Freq.: Daily Transplacental)) (View Methylprednisolone Review and Methylprednisolone Label ), TRIMETHOPRIM + SULFAMETHOXAZOLE ((transplacental)) (View Trimethoprim + Sulfamethoxazole Review and Trimethoprim + Sulfamethoxazole Label ), INSULIN (View Insulin Review and Insulin Label ). Patient was hospitalized.

6517163-4 | Accidental Overdose, Depression, Dermatitis Exfoliative, Psoriasis, Psoriatic Arthropathy, Suicidal Ideation
Adverse event was reported on Dec 09, 2009 by a Female patient taking Betamethasone (View Usage) (Dosage: ) was diagnosed with pustular psoriasis and. Location: FRANCE , 59 years of age, Patient experienced the following unwanted or unexpected effects: accidental overdose, depression (What is depression?), dermatitis exfoliative, psoriasis, psoriatic arthropathy, suicidal ideation. During the same period patient was treated with ULTRAVIOLET LIGHT (View Ultraviolet Light Review and Ultraviolet Light Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), ACITRETIN (View Acitretin Review and Acitretin Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ).

6499807-9 | Abnormal Behaviour, Coagulopathy, Cold Sweat, Fall, Haemorrhagic Stroke, Hypertension, Insomnia, Intracranial Aneurysm
on Dec 08, 2009 Male patient from UNITED STATES , 72 years of age, weighting 299.9 lb, was diagnosed with neuropathy peripheral, pain in extremity, blood pressure (What is blood pressure?), insomnia, urinary tract disorder and was treated with Betamethasone (View Usage). Patient had the following side effects: abnormal behaviour, coagulopathy, cold sweat, fall (What is fall?), haemorrhagic stroke, hypertension, insomnia, intracranial aneurysm. Betamethasone dosage: 50 Mg, Prn, Top. During the same period patient was treated with FENTANYL 100 (50 Mcg, Tder) (View Fentanyl-100 Review and Fentanyl-100 Label ), FENTANYL 100 (50 Mcg, Tder) (View Fentanyl-100 Review and Fentanyl-100 Label ), METOPROLOL TARTRATE (50 Mg, Bid, Po) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), HYDROCODONE BITARTRATE + ACETAMINOPHEN (6 Df, Qd, Po) (View Hydrocodone Bitartrate + Acetaminophen Review and Hydrocodone Bitartrate + Acetaminophen Label ), AMBIEN (10 Mg, Prn, Po) (View Ambien Review and Ambien Label ), AMMONIUM LACTATE (400 Mg, Bid, Po) (View Ammonium Lactate Review and Ammonium Lactate Label ), UROXATRAL (10 Mg, Qd, Po) (View Uroxatral Review and Uroxatral Label ), OXYCONTIN (40 Mg, Prn, Po) (View Oxycontin Review and Oxycontin Label ). Patient was hospitalized.

6463208-X | Foetal Growth Retardation, Pelvic Kidney, Premature Baby, Small For Dates Baby, Solitary Kidney
on Nov 06, 2009 Female patient from UNITED KINGDOM , weighting 3.17 lb, was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: foetal growth retardation, pelvic kidney, premature baby, small for dates baby, solitary kidney. Betamethasone dosage: Trpl. During the same period patient was treated with PREDNISOLONE (Trpl) (View Prednisolone Review and Prednisolone Label ), METHYLPREDNISOLONE (Trpl) (View Methylprednisolone Review and Methylprednisolone Label ), CYCLOPHOSPHAMIDE (Trpl) (View Cyclophosphamide Review and Cyclophosphamide Label ), TRIMETHOPRIM + SULFAMETHOXAZOLE (Trpl) (View Trimethoprim + Sulfamethoxazole Review and Trimethoprim + Sulfamethoxazole Label ).

6454661-6 | Aneurysm, Coagulopathy, Cold Sweat, Fall, Feeling Abnormal, Haemorrhagic Stroke, Hypertension, Initial Insomnia
Patient was taking Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: aneurysm (What is aneurysm?), coagulopathy, cold sweat, fall (What is fall?), feeling abnormal, haemorrhagic stroke, hypertension, initial insomnia on Nov 13, 2009 from UNITED STATES Additional patient health information: Male patient , 72 years of age, weighting 299.9 lb, was diagnosed with neuropathy peripheral, blood pressure (What is blood pressure?), pain (What is pain?), insomnia, micturition disorder, diabetes mellitus and. Betamethasone dosage: 50 Mg; Prn; Top. During the same period patient was treated with FENTANYL (50 Mcg; Tder) (View Fentanyl Review and Fentanyl Label ), METOPROLOL (50 Mg; Bid;po) (View Metoprolol Review and Metoprolol Label ), HYDROCODONE BITARTRATE + ACETAMINOPHEN (6 Df; Qd; Po) (View Hydrocodone Bitartrate + Acetaminophen Review and Hydrocodone Bitartrate + Acetaminophen Label ), AMBIEN (10 Mg; Prn; Po) (View Ambien Review and Ambien Label ), AMMONIUM LACTATE (400 Mg; Bid; Top) (View Ammonium Lactate Review and Ammonium Lactate Label ), UROXATRAL (10 Mg; Qd; Po) (View Uroxatral Review and Uroxatral Label ), OXYCONTIN (40 Mg; Prn; Po) (View Oxycontin Review and Oxycontin Label ), NOVALAC (15 Gm;tid; Sc) (View Novalac Review and Novalac Label ). Patient was hospitalized.

6442388-6 | Abnormal Behaviour, Coagulopathy, Diabetes Mellitus, Fall, Haemorrhagic Stroke, Hypertension, Initial Insomnia, Neuropathy Peripheral
Adverse event was reported on Nov 06, 2009 by a Male patient taking Betamethasone (View Usage) (Dosage: 50 Mg; Prn; Top) was diagnosed with neuropathy peripheral, pain in extremity, blood pressure (What is blood pressure?), insomnia, dysuria and. Location: UNITED STATES , 72 years of age, weighting 299.9 lb, Patient had the following side effects: abnormal behaviour, coagulopathy, diabetes mellitus, fall (What is fall?), haemorrhagic stroke, hypertension, initial insomnia, neuropathy peripheral. During the same period patient was treated with FENTANYL 100 (50 Mcg; Tder) (View Fentanyl-100 Review and Fentanyl-100 Label ), FENTANYL 100 (50 Mcg; Tder) (View Fentanyl-100 Review and Fentanyl-100 Label ), METOPROLOL (50 Mg; Bid; Po) (View Metoprolol Review and Metoprolol Label ), HYDROCODONE BITARTRATE + ACETAMINOPHEN (6 Df; Qd; Po) (View Hydrocodone Bitartrate + Acetaminophen Review and Hydrocodone Bitartrate + Acetaminophen Label ), AMBIEN (10 Mg; Prn; Po) (View Ambien Review and Ambien Label ), AMMONIUM LACTATE (400 Mg; Bid; Top) (View Ammonium Lactate Review and Ammonium Lactate Label ), UROXATRAL (10 Mg; Qd; Po) (View Uroxatral Review and Uroxatral Label ), OXYCONTIN (40 Mg; Prn; Po) (View Oxycontin Review and Oxycontin Label ). Patient was hospitalized.

6426534-6 | Headache, Lymphadenopathy
on Oct 26, 2009 Male patient from FRANCE , child 3 years of age, weighting 36.38 lb, was diagnosed with pyrexia and was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: headache (What is headache?), lymphadenopathy. Betamethasone dosage: 40 Gtt; Bid; Po. During the same period patient was treated with ADVIL (1 Df; Q8h; Po) (View Advil Review and Advil Label ), ASPEGIC 1000 (1 Df; Tid; Po) (View Aspegic 1000 Review and Aspegic 1000 Label ). Patient was hospitalized.

6411151-4 | Headache, Lymphadenopathy, No Therapeutic Response
on Oct 12, 2009 Male patient from FRANCE , child 3 years of age, weighting 36.38 lb, was diagnosed with pyrexia and was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: headache (What is headache?), lymphadenopathy, no therapeutic response. Betamethasone dosage: 40 Gtt; Bid; Po. During the same period patient was treated with ADVIL (1 Df; Q8h, Po) (View Advil Review and Advil Label ), ASPEGIC 1000 (1 Df; Tid; Po) (View Aspegic 1000 Review and Aspegic 1000 Label ). Patient was hospitalized.

6404904-X | Condition Aggravated
Patient was taking Betamethasone (View Usage). Patient had the following side effects: condition aggravated on Oct 08, 2009 from FRANCE Additional patient health information: Female patient , 70 years of age, was diagnosed with pain (What is pain?) and. Betamethasone dosage: 3 Mg; Qd; Po. During the same period patient was treated with PREDNISONE (20 Mg; Qd; Po) (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

6388308-4 | Amyotrophy, Autonomic Nervous System Imbalance, Bacterial Infection, Blood Albumin Decreased, Blood Thyroid Stimulating Hormone Increased, Cushing's Syndrome, Ecchymosis, Fluid Retention
Adverse event was reported on Sep 24, 2009 by a Female patient taking Betamethasone (View Usage) (Dosage: 4 Mg; Po) . Location: FRANCE , 75 years of age, After Betamethasone was administered, patient had the following side effects: amyotrophy, autonomic nervous system imbalance, bacterial infection (What is bacterial infection?), blood albumin decreased, blood thyroid stimulating hormone increased, cushing's syndrome, ecchymosis, fluid retention. During the same period patient was treated with SOLUPRED (PREDNISOLONE SODIUM SULFOBENZOATE) (40 Mg;qd) (View Solupred (prednisolone Sodium Sulfobenzoate) Review and Solupred (prednisolone Sodium Sulfobenzoate) Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), AMLOR (View Amlor Review and Amlor Label ), TAHOR (View Tahor Review and Tahor Label ), ATARAX (View Atarax Review and Atarax Label ), CYSTINE B6 (View Cystine B6 Review and Cystine B6 Label ), PORPOFAN (View Porpofan Review and Porpofan Label ), FUCIDINE CAP (View Fucidine Cap Review and Fucidine Cap Label ). Patient was hospitalized.

6376091-8 | Dermatitis, Erythema, Fluid Retention, Hypernatraemia, Increased Tendency To Bruise, Oedema, Oedema Peripheral, Overdose, Photosensitivity Reaction
on Sep 17, 2009 Female patient from FRANCE , 75 years of age, was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: dermatitis, erythema, fluid retention, hypernatraemia, increased tendency to bruise, oedema, oedema peripheral, overdose, photosensitivity reaction. Betamethasone dosage: 4 Mg. During the same period patient was treated with SOLUPRED (PREDNISOLONE SODIUM SULFOBENZOATE) (40 Mg; Qd) (View Solupred (prednisolone Sodium Sulfobenzoate) Review and Solupred (prednisolone Sodium Sulfobenzoate) Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), AMLOR (View Amlor Review and Amlor Label ), TAHOR (View Tahor Review and Tahor Label ), ATARAX (View Atarax Review and Atarax Label ), CYSTINE B6 (View Cystine B6 Review and Cystine B6 Label ), PROPOFAN (View Propofan Review and Propofan Label ), FUCIDINE CAP (View Fucidine Cap Review and Fucidine Cap Label ). Patient was hospitalized.

6355705-2 | Anaphylactic Reaction, Diarrhoea, Hypersensitivity, Syncope
on Sep 03, 2009 Female patient from GREECE , 60 years of age, weighting 141.1 lb, was treated with Betamethasone (View Usage). Patient had the following side effects: anaphylactic reaction, diarrhoea, hypersensitivity, syncope. Betamethasone dosage: . During the same period patient was treated with MEDROL (View Medrol Review and Medrol Label ), XYLOCAINE (View Xylocaine Review and Xylocaine Label ).

6354791-3 | Coma, Convulsion, Hypoxia, Laryngeal Obstruction, Loss Of Consciousness, Respiratory Distress
Patient was taking Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: coma, convulsion, hypoxia, laryngeal obstruction, loss of consciousness, respiratory distress on Sep 04, 2009 from FRANCE Additional patient health information: Male patient , child 9 years of age, weighting 66.14 lb, was diagnosed with laryngitis and. Betamethasone dosage: 90 Gtt, Once, Po.

6342055-3 | Anaemia Neonatal, Caesarean Section, Cerebral Cyst, Hyperbilirubinaemia Neonatal, Hypernatraemia, Hypokalaemia, Neonatal Disorder, Neonatal Hypotension
Adverse event was reported on Aug 05, 2009 by a Female patient taking Betamethasone (View Usage) (Dosage: Trpl) was diagnosed with essential hypertension and. Location: SWITZERLAND , weighting 1.54 lb, Patient experienced the following unwanted or unexpected effects: anaemia neonatal, caesarean section, cerebral cyst, hyperbilirubinaemia neonatal, hypernatraemia, hypokalaemia, neonatal disorder, neonatal hypotension. During the same period patient was treated with NORVASC (Trpl) (View Norvasc Review and Norvasc Label ), TRANDATE (Trpl) (View Trandate Review and Trandate Label ), PENICILLIN G (Trpl) (View Penicillin G Review and Penicillin G Label ), ERYTHROCIN (Trpl) (View Erythrocin Review and Erythrocin Label ), GYNIPRAL (View Gynipral Review and Gynipral Label ). Patient was hospitalized.

6301562-X | Abasia, Blood Lactic Acid Increased, Dyspnoea, Fatigue, Glycosuria, Hyperglycaemia, Hypokalaemia, Hypophosphataemia, Myalgia
on Jul 31, 2009 Male patient from FRANCE , 22 years of age, was diagnosed with dyspnoea, asthma (What is asthma?) and was treated with Betamethasone (View Usage). Patient had the following side effects: abasia, blood lactic acid increased, dyspnoea, fatigue, glycosuria, hyperglycaemia, hypokalaemia, hypophosphataemia, myalgia. Betamethasone dosage: 2 Mg;bid;po. During the same period patient was treated with AIROMIR (SALBUTAMOL SULFATE) (1 Df;tid;inh) (View Airomir (salbutamol Sulfate) Review and Airomir (salbutamol Sulfate) Label ), SYMBICORT (2 Df;tid;inh) (View Symbicort Review and Symbicort Label ), AMOXICILLIN (1 Df;qd;po) (View Amoxicillin Review and Amoxicillin Label ), PHOLCODINE TAB (1 Df;tid;po) (View Pholcodine Tab Review and Pholcodine Tab Label ). Patient was hospitalized.

6287468-3 | Caesarean Section, Hiv Infection, Metrorrhagia, Premature Labour
on Jul 16, 2009 Female patient from SWITZERLAND , 33 years of age, was diagnosed with hiv infection (What is hiv infection?) and was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: caesarean section, hiv infection (What is hiv infection?), metrorrhagia, premature labour. Betamethasone dosage: . During the same period patient was treated with KALETRA (Qid) (View Kaletra Review and Kaletra Label ), COMBIVIR (Bid) (View Combivir Review and Combivir Label ), ZITHROMAX (250 Mg;tid) (View Zithromax Review and Zithromax Label ), AUGMENTIN (625 Mg;tid) (View Augmentin Review and Augmentin Label ), ISOTRETINOIN (Qd) (View Isotretinoin Review and Isotretinoin Label ), MAGNESIOCARD (View Magnesiocard Review and Magnesiocard Label ). Patient was hospitalized.

6285396-0 | Dermatitis Exfoliative, Face Oedema, Hypotension, Malaise
Patient was taking Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: dermatitis exfoliative, face oedema, hypotension, malaise on Jul 20, 2009 from FRANCE Additional patient health information: Female patient , 87 years of age, . Betamethasone dosage: 1 Df, Qd. Po. During the same period patient was treated with MOXIFLOXACIN HYDROCHLORIDE (400 Mg, Qd, Po) (View Moxifloxacin Hydrochloride Review and Moxifloxacin Hydrochloride Label ), CAPTOPRIL AND HYDROCHLOROTHIAZIDE (View Captopril And Hydrochlorothiazide Review and Captopril And Hydrochlorothiazide Label ). Patient was hospitalized.

6257759-0 | Condition Aggravated, Effusion, Lung Disorder, Pneumonia
Adverse event was reported on Jun 26, 2009 by a Female patient taking Betamethasone (View Usage) (Dosage: 1 Df; Qd; Po) was diagnosed with cough, pyrexia and. Location: FRANCE , weighting 22.05 lb, Patient had the following side effects: condition aggravated, effusion, lung disorder, pneumonia (What is pneumonia?). During the same period patient was treated with ADVIL (1 Df; Tid; Po) (View Advil Review and Advil Label ), HELICIDINE (HELICIDINE) (1 Df; Tid; Po) (View Helicidine (helicidine) Review and Helicidine (helicidine) Label ), NUREFLEX (IBUPROFEN) (1 Df; Tid; Po) (View Nureflex (ibuprofen) Review and Nureflex (ibuprofen) Label ). Patient was hospitalized.

6231058-5 | Spinal Myelogram Abnormal, Thrombocytopenia
on Mar 12, 2009 Female patient from FRANCE , 46 years of age, weighting 185.2 lb, was diagnosed with bronchitis (What is bronchitis?), breast cancer (What is breast cancer?) and was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: spinal myelogram abnormal, thrombocytopenia. Betamethasone dosage: Inh. During the same period patient was treated with NETROMYCIN (Inh) (View Netromycin Review and Netromycin Label ), PAROXETINE HYDROCHLORIDE (40 Mg; Qd; Po, 20 Mg; Qd; Po) (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ), TRIPTORELIN PAMOATE (0.011 Df; Qid; Im) (View Triptorelin Pamoate Review and Triptorelin Pamoate Label ), ABUFENE (BETA ALANINE) (Po) (View Abufene (beta-alanine) Review and Abufene (beta-alanine) Label ), SURBRONC (AMBROXOL HYDROCHLORIDE) (Inh) (View Surbronc (ambroxol Hydrochloride) Review and Surbronc (ambroxol Hydrochloride) Label ), GOMENOL (CON.) (View Gomenol (con.) Review and Gomenol (con.) Label ). Patient was hospitalized.

6217038-4 | Cheilitis, Chlamydia Identification Test Positive, Genital Disorder Female, Hyperthermia, Oral Disorder
on May 28, 2009 Female patient from FRANCE , 70 years of age, was diagnosed with pain (What is pain?) and was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: cheilitis, chlamydia identification test positive, genital disorder female, hyperthermia, oral disorder. Betamethasone dosage: 3 Mg; Qd; Po. During the same period patient was treated with PREDNISONE TAB (20 Mg; Qd; Po) (View Prednisone Tab Review and Prednisone Tab Label ). Patient was hospitalized.

6211565-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blister, Blood Immunoglobulin G Decreased, Blood Lactate Dehydrogenase Increased, Blood Pressure Decreased, Blood Urea Increased, Bundle Branch Block Right, Condition Aggravated
Patient was taking Betamethasone (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blister, blood immunoglobulin g decreased, blood lactate dehydrogenase increased, blood pressure decreased, blood urea increased, bundle branch block right, condition aggravated on May 22, 2009 from JAPAN Additional patient health information: Female patient , 57 years of age, . Betamethasone dosage: 5 Mg;qd;po; 0.5 Mg;qd;po. During the same period patient was treated with PREDNISOLONE (50 Mg;qd;po) (View Prednisolone Review and Prednisolone Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), VENOGLOBULIN /00025201/ (View Venoglobulin /00025201/ Review and Venoglobulin /00025201/ Label ), ALLELOCK (View Allelock Review and Allelock Label ), ANTEBATE (View Antebate Review and Antebate Label ).

6207787-6 | Blood Pressure Decreased, Cardiac Enzymes Increased, Electrocardiogram Abnormal, Hepatic Function Abnormal, Malaise, Myocarditis, Ventricular Tachycardia
Adverse event was reported on May 13, 2009 by a Female patient taking Betamethasone (View Usage) (Dosage: 5 Mg;qd;po; 0.5 Mg;qd;po) . Location: JAPAN , 57 years of age, After Betamethasone was administered, patient had the following side effects: blood pressure decreased, cardiac enzymes increased, electrocardiogram abnormal, hepatic function abnormal, malaise, myocarditis, ventricular tachycardia. During the same period patient was treated with PREDNISOLONE (50 Mg; Qd; Po) (View Prednisolone Review and Prednisolone Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), VENOGLOBULIN (View Venoglobulin Review and Venoglobulin Label ).

6196689-X | Unevaluable Event
on May 13, 2009 Female patient from JAPAN , 57 years of age, was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: unevaluable event. Betamethasone dosage: 5 Mg;po. During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), VENOGLOBULIN (View Venoglobulin Review and Venoglobulin Label ).

6181321-1 | Abasia, Dyspnoea, Fatigue, Glycosuria, Hyperglycaemia, Hypokalaemia, Hypophosphataemia, Myalgia, Pain In Extremity
on Apr 23, 2009 Male patient from FRANCE , 22 years of age, was diagnosed with dyspnoea, asthma (What is asthma?) and was treated with Betamethasone (View Usage). Patient had the following side effects: abasia, dyspnoea, fatigue, glycosuria, hyperglycaemia, hypokalaemia, hypophosphataemia, myalgia, pain in extremity. Betamethasone dosage: 2 Mg; Bid; Po. During the same period patient was treated with AIROMIR (SALBUTAMOL SULFATE) (1 Df; Tid; Inh) (View Airomir (salbutamol Sulfate) Review and Airomir (salbutamol Sulfate) Label ), SYMBICORT (2 Df; Tid; Inh) (View Symbicort Review and Symbicort Label ), AMOXICILLIN (1 Df; Qd; Po) (View Amoxicillin Review and Amoxicillin Label ), PHOLCODINE TAB (1 Df; Tid; Po) (View Pholcodine Tab Review and Pholcodine Tab Label ). Patient was hospitalized.

6129560-X | Bone Marrow Myelogram Abnormal, Thrombocytopenia
Patient was taking Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: bone marrow myelogram abnormal, thrombocytopenia on Mar 12, 2009 from FRANCE Additional patient health information: Female patient , 46 years of age, weighting 185.2 lb, was diagnosed with bronchitis (What is bronchitis?), breast cancer (What is breast cancer?) and. Betamethasone dosage: Inh. During the same period patient was treated with NETROMYCIN (Inh) (View Netromycin Review and Netromycin Label ), PAROXETINE HYDROCHLORIDE (40 Mg;qd;po; 20 Mg;qd;po) (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ), TRIPTORELIN PAMOATE (0.011 Df;qid;im) (View Triptorelin Pamoate Review and Triptorelin Pamoate Label ), ABUFENE (BETA ALANINE) (Po) (View Abufene (beta-alanine) Review and Abufene (beta-alanine) Label ), SURBRONC (AMBROXOL HYDROCHLORIDE) (Inh) (View Surbronc (ambroxol Hydrochloride) Review and Surbronc (ambroxol Hydrochloride) Label ), GOMENOL (View Gomenol Review and Gomenol Label ). Patient was hospitalized.

6125214-4 | Abnormal Faeces, Diarrhoea, Gastritis, Haematochezia, Middle Insomnia, Oesophagitis, Rectal Haemorrhage
Adverse event was reported on Mar 10, 2009 by a Male patient taking Betamethasone (View Usage) (Dosage: 150 Gtt; Qd; Po ; 300 Gtt; Od; Po) was diagnosed with viral pharyngitis and. Location: FRANCE , child 4 years of age, weighting 35.27 lb, Patient experienced the following unwanted or unexpected effects: abnormal faeces, diarrhoea, gastritis, haematochezia, middle insomnia, oesophagitis, rectal haemorrhage. During the same period patient was treated with ADVIL (View Advil Review and Advil Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

6054887-X | Bronchiolitis, Dyspnoea, Hypophagia, Nasal Congestion, Respiratory Disorder
on Jan 16, 2009 Male patient from FRANCE , weighting 16.76 lb, was diagnosed with laryngitis and was treated with Betamethasone (View Usage). Patient had the following side effects: bronchiolitis, dyspnoea, hypophagia, nasal congestion, respiratory disorder. Betamethasone dosage: ; Po. During the same period patient was treated with BRONCHOKOD (CARBOCISTEINE) (0.5 Df; Bid; Po) (View Bronchokod (carbocisteine) Review and Bronchokod (carbocisteine) Label ). Patient was hospitalized.

6037787-0 | Acute Sinusitis, Anxiety, Cyst, Electrocardiogram Qt Prolonged, Flushing, Hyperhidrosis, Infection
on Jan 05, 2009 Female patient from NETHERLANDS , 47 years of age, was diagnosed with acute sinusitis, cyst and was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: acute sinusitis, anxiety (What is anxiety?), cyst, electrocardiogram qt prolonged, flushing, hyperhidrosis, infection (What is infection?). Betamethasone dosage: 0.5 Mg;qd; Acute Sinusitis, Maxillary. During the same period patient was treated with AVELOX (400 Mg;qd;) (View Avelox Review and Avelox Label ), PRIADEL (LITHIUM) (LITHIUM CARBONATE) (400 Mg;ttd; 400 Mg;bid) (View Priadel (lithium) (lithium Carbonate) Review and Priadel (lithium) (lithium Carbonate) Label ), METAMUCIL (View Metamucil Review and Metamucil Label ). Patient was hospitalized.

6025195-8 | Diabetic Hyperosmolar Coma, Diabetic Ketoacidosis, Hypovolaemic Shock, Renal Failure Acute
Patient was taking Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: diabetic hyperosmolar coma, diabetic ketoacidosis, hypovolaemic shock, renal failure acute on Dec 19, 2008 from FRANCE Additional patient health information: Female patient , 45 years of age, was diagnosed with lung infection, schizophrenia and. Betamethasone dosage: Po. During the same period patient was treated with ZYPREXA (20 Mg, Qd; Po) (View Zyprexa Review and Zyprexa Label ), RULID (ROXITHROMYCIN) (Po) (View Rulid (roxithromycin) Review and Rulid (roxithromycin) Label ), TAHOR (View Tahor Review and Tahor Label ). Patient was hospitalized.

6024141-0 | Constipation, Diabetes Mellitus Inadequate Control, Hypoglycaemia
Adverse event was reported on Dec 08, 2008 by a Female patient taking Betamethasone (View Usage) (Dosage: Po) was diagnosed with renal cell carcinoma and. Location: SWEDEN , 67 years of age, weighting 145.5 lb, Patient had the following side effects: constipation (What is constipation?), diabetes mellitus inadequate control, hypoglycaemia. During the same period patient was treated with SU 011248 (SUNITINIB MALATE) (NO PREF. NAME) (12.5 Mg;tid; Po) (View Su 011248 (sunitinib Malate) (no Pref. Name) Review and Su 011248 (sunitinib Malate) (no Pref. Name) Label ), MORPHINE SULFATE (View Morphine Sulfate Review and Morphine Sulfate Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), CANDESARTAN (View Candesartan Review and Candesartan Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ). Patient was hospitalized.

5996628-8 | Abdominal Pain, Caesarean Section, Cholestasis, Faeces Discoloured, Premature Rupture Of Membranes, Pruritus
on Nov 18, 2008 Female patient from CANADA , 37 years of age, was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), caesarean section, cholestasis, faeces discoloured, premature rupture of membranes, pruritus. Betamethasone dosage: . During the same period patient was treated with DIGOXIN (.5 Mg, Oral) (View Digoxin Review and Digoxin Label ), SOTALOL HCL (160 Mg/ Twice Per Day/ Oral) (View Sotalol Hcl Review and Sotalol Hcl Label ), ACTIGALL (View Actigall Review and Actigall Label ).

5996601-X | Breech Presentation, Caesarean Section, Foetal Hypokinesia, Hydrops Foetalis, Premature Rupture Of Membranes, Tachycardia Foetal
on Nov 18, 2008 Female patient from CANADA , weighting 7.30 lb, was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: breech presentation, caesarean section, foetal hypokinesia, hydrops foetalis, premature rupture of membranes, tachycardia foetal. Betamethasone dosage: Transplacentary. During the same period patient was treated with LANOXIN (Transplacentary) (View Lanoxin Review and Lanoxin Label ), SOTALOL HCL (Transplacentary) (View Sotalol Hcl Review and Sotalol Hcl Label ), ACTIGALL (Transplacentary) (View Actigall Review and Actigall Label ). Patient was hospitalized.

5976809-X | Hemiparesis, Hypertensive Crisis
Patient was taking Betamethasone (View Usage). Patient had the following side effects: hemiparesis, hypertensive crisis on Nov 18, 2008 from FRANCE Additional patient health information: Female patient , 54 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and. Betamethasone dosage: 4 Mg; Qd; Po. During the same period patient was treated with BETAMETHASONE SODIUM PHOSPHATE (8 Mg; ; Iv) (View Betamethasone Sodium Phosphate Review and Betamethasone Sodium Phosphate Label ), ACTEMRA (TOCILIZUMAB) (400 Mg; ; Iv) (View Actemra (tocilizumab) Review and Actemra (tocilizumab) Label ), IMUREL (View Imurel Review and Imurel Label ), NEXIUM (View Nexium Review and Nexium Label ). Patient was hospitalized.

5939491-3 | Laboratory Test Abnormal, Leukocytosis, Neutrophilia
Adverse event was reported on Oct 17, 2008 by a Male patient taking Betamethasone (View Usage) (Dosage: 6 Mg, Qd, Intravenous; 4mg, Qd) was diagnosed with dermatitis atopic and. Location: TAIWAN, PROVINCE OF CHINA , 13 years of age, weighting 147.7 lb, After Betamethasone was administered, patient had the following side effects: laboratory test abnormal, leukocytosis, neutrophilia. During the same period patient was treated with HYDROCORTISONE (200 Mg, Qd, Intravenous) (View Hydrocortisone Review and Hydrocortisone Label ). Patient was hospitalized.

5878605-0 | Confusional State, Malaise, Pyrexia
on Sep 03, 2008 Female patient from FRANCE , child 2. years of age, was diagnosed with ear pain and was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, malaise, pyrexia. Betamethasone dosage: 120 Gtt; Once; Po. Patient was hospitalized.

5775352-0 | Anaemia, Cardiac Murmur, Gastric Ulcer Haemorrhage, Gastrointestinal Haemorrhage, Haematemesis, Heart Rate Increased, Melaena, Pallor, Pyrexia
on Jun 09, 2008 Male patient from FRANCE , child 4 years of age, weighting 33.95 lb, was diagnosed with cough, rhinorrhoea and was treated with Betamethasone (View Usage). Patient had the following side effects: anaemia, cardiac murmur, gastric ulcer haemorrhage, gastrointestinal haemorrhage, haematemesis, heart rate increased, melaena, pallor, pyrexia. Betamethasone dosage: 170 Gtt;qd;po. During the same period patient was treated with ADVIL (100 Mg;tid;po) (View Advil Review and Advil Label ), PNEUMOREL (FENS PIRIDE HYDROCHLORIDE) (Po) (View Pneumorel (fens Piride Hydrochloride) Review and Pneumorel (fens Piride Hydrochloride) Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

5766488-9 | Abortion Missed, Bronchopulmonary Dysplasia, Caesarean Section, Cerebral Haemorrhage Neonatal, Glucose-6-phosphate Dehydrogenase Deficiency, Necrotising Enterocolitis Neonatal, Neonatal Respiratory Distress Syndrome, Premature Baby
Patient was taking Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: abortion missed, bronchopulmonary dysplasia, caesarean section, cerebral haemorrhage neonatal, glucose-6-phosphate dehydrogenase deficiency, necrotising enterocolitis neonatal, neonatal respiratory distress syndrome, premature baby on May 27, 2008 from FRANCE Additional patient health information: Male patient , weighting 2.71 lb, was diagnosed with abortion induced and. Betamethasone dosage: Trpl. During the same period patient was treated with MIFEGYNE (MIFEPRISTONE) (1 Df; Once) (View Mifegyne (mifepristone) Review and Mifegyne (mifepristone) Label ), KETOPROFEN (1 Df;once;trpl) (View Ketoprofen Review and Ketoprofen Label ), NICARDIPINE HCL (View Nicardipine Hcl Review and Nicardipine Hcl Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), FLAGYL (View Flagyl Review and Flagyl Label ), CYTOTEC (4 Df; Once; Trpl) (View Cytotec Review and Cytotec Label ). Patient was hospitalized.

5762133-7 | Disseminated Intravascular Coagulation, Infection, Neoplasm Progression, Platelet Count Decreased, Pneumonia Aspiration
Adverse event was reported on Jun 02, 2008 by a Female patient taking Betamethasone (View Usage) (Dosage: ; Po) was diagnosed with anaplastic astrocytoma and. Location: JAPAN , 64 years of age, weighting 83.78 lb, Patient experienced the following unwanted or unexpected effects: disseminated intravascular coagulation, infection (What is infection?), neoplasm progression, platelet count decreased, pneumonia aspiration. During the same period patient was treated with TEMODAL (150 Mg/m2; Qd;, 200 Mg/m2; Qd;) (View Temodal Review and Temodal Label ), SULFAMETHOXAZOLE AND TRIMETHOPRIM (View Sulfamethoxazole And Trimethoprim Review and Sulfamethoxazole And Trimethoprim Label ), EXCEGRAN (View Excegran Review and Excegran Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), MYSTAN (View Mystan Review and Mystan Label ), BIOFERMIN (View Biofermin Review and Biofermin Label ).

5757733-4 | Bronchitis, Erythema, Inflammation, Leukocytosis, Purpura, Rash Morbilliform, Rash Pruritic, Rash Pustular, Rib Fracture
on May 23, 2008 Male patient from FRANCE , 89 years of age, was diagnosed with bronchitis (What is bronchitis?) and was treated with Betamethasone (View Usage). Patient had the following side effects: bronchitis (What is bronchitis?), erythema, inflammation, leukocytosis, purpura, rash morbilliform, rash pruritic, rash pustular, rib fracture. Betamethasone dosage: Po. During the same period patient was treated with AMOXICILLIN (Po) (View Amoxicillin Review and Amoxicillin Label ), VENTOLIN (Inh) (View Ventolin Review and Ventolin Label ), BIOCALYPTOL (PHOLCODINE) (View Biocalyptol (pholcodine) Review and Biocalyptol (pholcodine) Label ), DOLIPRANE (View Doliprane Review and Doliprane Label ), CASODEX (View Casodex Review and Casodex Label ), VOLTAREN (View Voltaren Review and Voltaren Label ), TAHOR (View Tahor Review and Tahor Label ), ISKEDYL (View Iskedyl Review and Iskedyl Label ). Patient was hospitalized.

5724459-2 | Erythema, Productive Cough, Pruritus, Pyrexia, Rash Maculo-papular
on Apr 22, 2008 Male patient from FRANCE , 46 years of age, was diagnosed with sinusitis (What is sinusitis?) and was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: erythema, productive cough, pruritus, pyrexia, rash maculo-papular. Betamethasone dosage: Po. During the same period patient was treated with CEFPODOXIME PROXETIL (Po) (View Cefpodoxime Proxetil Review and Cefpodoxime Proxetil Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), ACETYLCYSTEINE (Po) (View Acetylcysteine Review and Acetylcysteine Label ). Patient was hospitalized.

5714321-3 | Arthralgia, Epstein-barr Virus Infection, Erythema Infectiosum, Inflammation, Localised Oedema, Monocyte Count Increased, Neutrophil Count Increased, Oedema Peripheral
Patient was taking Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, epstein-barr virus infection, erythema infectiosum, inflammation, localised oedema, monocyte count increased, neutrophil count increased, oedema peripheral on Apr 14, 2008 from FRANCE Additional patient health information: Female patient , 48 years of age, was diagnosed with rash (What is rash?), pharyngolaryngeal pain, influenza and. Betamethasone dosage: 4 Mg; Qd; Po. During the same period patient was treated with AERIUS (DESLORATADINE) (DESLORATADTNE) (5 Mg;qd;po) (View Aerius (desloratadine) (desloratadtne) Review and Aerius (desloratadine) (desloratadtne) Label ), MONOZECLAR (CLARITHROMYCIN) (500 Mg; Qd; Po) (View Monozeclar (clarithromycin) Review and Monozeclar (clarithromycin) Label ), KETOPROFEN (2 Df; Qd; Po) (View Ketoprofen Review and Ketoprofen Label ), IXPRIM (ULTRACET) (3 Df; Qd; Po) (View Ixprim (ultracet) Review and Ixprim (ultracet) Label ), ORBENIN CAP (2 Gm; Qd; Po) (View Orbenin Cap Review and Orbenin Cap Label ), VOLTAREN (150 Mg; Qd; Po) (View Voltaren Review and Voltaren Label ), PREDNISOLONE (20 Mg; Qd; Po) (View Prednisolone Review and Prednisolone Label ), PYOSTACINE (PRISTINAMYCIN) (2 Df; Tid; Po) (View Pyostacine (pristinamycin) Review and Pyostacine (pristinamycin) Label ). Patient was hospitalized.

5679795-5 | Alanine Aminotransferase Increased, Liver Disorder
Adverse event was reported on Mar 12, 2008 by a Female patient taking Betamethasone (View Usage) (Dosage: 1.5 Mg; Qd; Po) was diagnosed with hepatitis b (What is hepatitis b?), prophylaxis and. Location: SPAIN , 70 years of age, Patient had the following side effects: alanine aminotransferase increased, liver disorder. During the same period patient was treated with KOBALNON (TERPRENONE) (TEPRENONE) (150 Mg; Qd; Po) (View Kobalnon (terprenone) (teprenone) Review and Kobalnon (terprenone) (teprenone) Label ). Patient was hospitalized.

5650062-9 | Angioedema, Bronchospasm, Dyspnoea, Respiratory Rate Increased, Stridor, Tracheitis, Urticaria
on Feb 21, 2008 Male patient from UNITED STATES , child 2 years of age, was diagnosed with bronchospasm, tracheitis and was treated with Betamethasone (View Usage). After Betamethasone was administered, patient had the following side effects: angioedema, bronchospasm, dyspnoea, respiratory rate increased, stridor, tracheitis, urticaria. Betamethasone dosage: 10 Mg; Once.

5612276-3 | Cardiac Murmur, Gastric Ulcer, Gastrointestinal Haemorrhage, Haemorrhagic Anaemia, Heart Rate Increased, Pyrexia, Thirst, Vomiting
on Jan 22, 2008 Male patient from FRANCE , child 4 years of age, weighting 33.95 lb, was diagnosed with rhinorrhoea and was treated with Betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac murmur, gastric ulcer, gastrointestinal haemorrhage, haemorrhagic anaemia, heart rate increased, pyrexia, thirst, vomiting. Betamethasone dosage: 170 Gtt;qd;po. During the same period patient was treated with ADVIL (100 Mg;tid;po) (View Advil Review and Advil Label ), PNEUMOREL (FENSPIRIDE HYDROCHLORIDE) (Po) (View Pneumorel (fenspiride Hydrochloride) Review and Pneumorel (fenspiride Hydrochloride) Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

5594575-7 | Balance Disorder, Diplopia, Dysarthria, Gait Disturbance
Patient was taking Betamethasone (View Usage). Patient had the following side effects: balance disorder, diplopia, dysarthria, gait disturbance on Jan 09, 2008 from FRANCE Additional patient health information: Female patient , child 10 years of age, . Betamethasone dosage: . During the same period patient was treated with CLONAZEPAM (10 Mg; Once; Po) (View Clonazepam Review and Clonazepam 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 Betamethasone 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 Betamethasone quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Betamethasone 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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Betamethasone Reactions
Abasia
Abnormal Behaviour
AbscessWhat is Abscess?
Alanine Aminotransferase Increased
Angioedema
AnxietyWhat is Anxiety?
Arthralgia
Asthenia
Brain Death
Burning Sensation
Caesarean Section
Candidiasis
Coagulopathy
Condition Aggravated
Dyspnoea
Erythema
Face Oedema
FallWhat is Fall?
Haemorrhagic Stroke
Hyperglycaemia
Hypertension
InfectionWhat is Infection?
Malaise
Oedema Peripheral
Premature Baby
Premature Rupture Of Membranes
Pruritus
Purpura
Pyrexia
Stevens-johnson Syndrome
Betamethasone 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 Betamethasone 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!