About this FactMed analysis covering adverse side effect reports of SEREVENT patients who developed ADRENALITIS.

FactMed provides MD-approved analysis to help both patients, researchers, and physicians accurately assess the risk profile for more than 20,000 different pharmaceutical products. The below report offers compiled information from Food & Drug Administration and FactMed user submissions. Between January 2004 and October 2012, 2 individuals taking SEREVENT reported ADRENALITIS to the FDA. A total of 6680 SEREVENT drug adverse event reaction reports were made with the FDA during this time period. Often the FDA only receives reports of the most critical and severe cases; these numbers may therefore underrepresent the complication rate of the medication.

FDA Research Report

Introduction This page is designed to help you determine the relationship, if any, between SEREVENT and ADRENALITIS. In doing so, we compare SEREVENT with other drugs that cause ADRENALITIS, to help you evaluate whether or not SEREVENT causes ADRENALITIS. Likewise, this page shows the most highly-reported side effects of SEREVENT, so you can see if ADRENALITIS ranks among SEREVENT's most well-known side effects.
Summary Statistics
Reports of SEREVENT causing ADRENALITIS: 2
Reports of any side effect of SEREVENT : 6680
Percentage of SEREVENT patients where ADRENALITIS is a reported side effect: 0.0299%

FDA reports of any drug causing ADRENALITIS : 27
Average percentage for all medicated patients where ADRENALITIS is reported as a complication: 0.0002%

Physician opinion on SEREVENT as adverse event culprit:

Overall opinion for all reports of this drug:
Most frequent diagnoses/indications for prescribing SEREVENT:
ASTHMA ( 1685 patients )
DRUG USE FOR UNKNOWN INDICATION ( 688 patients )
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 421 patients )
ILL-DEFINED DISORDER ( 228 patients )
EMPHYSEMA ( 114 patients )
PRODUCT USED FOR UNKNOWN INDICATION ( 107 patients )
DYSPNOEA ( 39 patients )
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 23 patients )
BRONCHITIS ( 15 patients )
BRONCHOSPASM ( 15 patients )
HYPERSENSITIVITY ( 11 patients )
BRONCHIECTASIS ( 9 patients )
COUGH ( 8 patients )
RESPIRATORY DISORDER ( 7 patients )
LUNG DISORDER ( 6 patients )
BRONCHITIS CHRONIC ( 6 patients )
LYMPHANGIOLEIOMYOMATOSIS ( 5 patients )
MYALGIA ( 5 patients )
ASTHMA EXERCISE INDUCED ( 4 patients )
WHEEZING ( 3 patients )
NASOPHARYNGITIS ( 3 patients )
OBSTRUCTIVE AIRWAYS DISORDER ( 3 patients )
PULMONARY FIBROSIS ( 3 patients )
CHEST DISCOMFORT ( 3 patients )
CHRONIC RESPIRATORY FAILURE ( 3 patients )
CYSTIC FIBROSIS LUNG ( 3 patients )
RESTRICTIVE PULMONARY DISEASE ( 2 patients )
MULTIPLE ALLERGIES ( 2 patients )
DRUG EFFECT DECREASED ( 2 patients )
INTERSTITIAL LUNG DISEASE ( 2 patients )
RHEUMATOID ARTHRITIS ( 2 patients )
PAIN ( 2 patients )
PULMONARY RADIATION INJURY ( 2 patients )
LUNG TRANSPLANT ( 1 patients )
CHRONIC SINUSITIS ( 1 patients )
CYSTIC FIBROSIS ( 1 patients )
ASTHMA PROPHYLAXIS ( 1 patients )
FIBROSIS ( 1 patients )
REFLUX OESOPHAGITIS ( 1 patients )
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 patients )
RESPIRATORY FAILURE ( 1 patients )
LUNG INJURY ( 1 patients )
ASBESTOSIS ( 1 patients )
OBLITERATIVE BRONCHIOLITIS ( 1 patients )
BRONCHIAL OBSTRUCTION ( 1 patients )
PROPHYLAXIS ( 1 patients )
INHALATION THERAPY ( 1 patients )
( 0 patients )
Drugs with high FDA adverse event association with ADRENALITIS:

TRUVADA (7 patients)
VALGANCICLOVIR (6 patients)
DURAGESIC (6 patients)
METHOTREXATE (5 patients)
FOLIC ACID (5 patients)
ENBREL (5 patients)
BYETTA (4 patients)
COTRIM (4 patients)
FLUCONAZOLE (4 patients)
FAMOTIDINE (4 patients)
LOPINAVIR/RITONAVIR (3 patients)
URSODIOL (3 patients)
RIBAVIRIN (3 patients)
PEGASYS (3 patients)
AZITHROMYCIN (3 patients)
INCIVEK (3 patients)
DYAZIDE (2 patients)
VENOSTASIN (THIAMINE HYDROCHLORIDE, HORSE CHESTNUT EXTRACT) (2 patients)
VALGANCICLOVIR HCL (2 patients)
ADVAIR DISKUS 100/50 (2 patients)
SULFAMETHOXAZOLE AND TRIMETHOPRIM (2 patients)
DDAVP (2 patients)
FLOVENT (2 patients)
STEROIDS NOS (2 patients)
CYCLOSPORINE (2 patients)
GOLIMUMAB (2 patients)
SINGULAIR (2 patients)
BAKTAR (2 patients)
KALETRA (2 patients)
SEREVENT (2 patients)
LISINOPRIL (2 patients)
SANASTHMYL (BECLOMETASONE DIPROPIONATE) (2 patients)
LOPINAVIR AND RITONAVIR (2 patients)
ZOLOFT (2 patients)
METFORMIN HCL (2 patients)
AMITRIPTYLINE HYDROCHLORIDE (2 patients)
METOCLOPRAMIDE (2 patients)
MOVICOL (MACROGOL, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM BICARBO (2 patients)
NITROGLYCERIN (2 patients)
REGLAN (2 patients)
OXIS (FORMOTEROL) (2 patients)
PRILOSEC (2 patients)
ANTI-ASTHMATICS (2 patients)
OXYCODONE HCL (2 patients)
PANTOPRAZOLE SODIUM (2 patients)
OXYCODON KAPSELN 5MG(OXY IR CAPSULE 5 MG) (1 patients)
OXYCODON KAPSELN 5MG (OXY IR CAPSULE 5 MG)IR CAPSULE (1 patients)
RAMIPRIL (1 patients)
NORVIR (1 patients)
RETROVIR (1 patients)
AZITHROMYC (1 patients)
LOPINAVIR + RITONAVIR (LOPINAVIR + RITONAVIR) (1 patients)
SANDIMMUNE (1 patients)
LAMIVUDINE (1 patients)
IBUPROFEN (ADVIL) (1 patients)
DARUNAVIR ETHANOLATE (1 patients)
EPIVIR (1 patients)
DEPO-PROVERA (1 patients)
URSODEOXYCHOLIC ACID (1 patients)
ADRENOCORTICOTROPHIC HORMONE (1 patients)
ACETAMINOPHEN (1 patients)
EFFEXOR (1 patients)
EFALIZUMAB (1 patients)
ZIAGEN (1 patients)
ZIDOVUDINE (1 patients)
ABACAVIR (1 patients)
Most common side effects for patients taking SEREVENT:
DRUG INEFFECTIVE (973 patients)
DYSPNOEA (900 patients)
ASTHMA (785 patients)
PHARMACEUTICAL PRODUCT COMPLAINT (407 patients)
COUGH (349 patients)
NAUSEA (315 patients)
CHEST PAIN (301 patients)
PNEUMONIA (301 patients)
DEATH (297 patients)
DIZZINESS (289 patients)
ANXIETY (278 patients)
PAIN (277 patients)
HEADACHE (269 patients)
FATIGUE (249 patients)
DEPRESSION (236 patients)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE (233 patients)
CHEST DISCOMFORT (229 patients)
WHEEZING (225 patients)
VOMITING (220 patients)
ASTHENIA (209 patients)
HYPERTENSION (207 patients)
PYREXIA (201 patients)
INSOMNIA (192 patients)
OEDEMA PERIPHERAL (191 patients)
DIARRHOEA (186 patients)
MYOCARDIAL INFARCTION (181 patients)
DRY MOUTH (171 patients)
CARDIAC FAILURE CONGESTIVE (170 patients)
BRONCHITIS (168 patients)
FALL (166 patients)
PRODUCT QUALITY ISSUE (165 patients)
BACK PAIN (151 patients)
PALPITATIONS (151 patients)
PAIN IN EXTREMITY (149 patients)
CONDITION AGGRAVATED (148 patients)
HEART RATE INCREASED (146 patients)
CONSTIPATION (146 patients)
ARTHRALGIA (145 patients)
TREMOR (144 patients)
RASH (143 patients)
MALAISE (143 patients)
WEIGHT DECREASED (140 patients)
ATRIAL FIBRILLATION (135 patients)
DYSPHONIA (133 patients)
ANAEMIA (129 patients)
MUSCLE SPASMS (125 patients)
CEREBROVASCULAR ACCIDENT (124 patients)
CORONARY ARTERY DISEASE (123 patients)
RESPIRATORY FAILURE (122 patients)
TACHYCARDIA (122 patients)
ABDOMINAL PAIN (120 patients)
INJURY (114 patients)
BLOOD PRESSURE INCREASED (109 patients)
WEIGHT INCREASED (109 patients)
SOMNOLENCE (109 patients)
PRURITUS (107 patients)
URINARY TRACT INFECTION (106 patients)
CARDIAC ARREST (106 patients)
MYALGIA (104 patients)
VISION BLURRED (104 patients)
PHARYNGOLARYNGEAL PAIN (103 patients)
CARDIO-RESPIRATORY ARREST (101 patients)
HYPOTENSION (101 patients)
RENAL FAILURE ACUTE (99 patients)
THROAT IRRITATION (98 patients)
RENAL FAILURE (97 patients)
GASTROOESOPHAGEAL REFLUX DISEASE (96 patients)
FEELING ABNORMAL (93 patients)
SINUSITIS (93 patients)
UPPER RESPIRATORY TRACT INFECTION (89 patients)
LOSS OF CONSCIOUSNESS (88 patients)
HYPERSENSITIVITY (87 patients)
ADVERSE EVENT (86 patients)
EMPHYSEMA (85 patients)
CONVULSION (84 patients)
EMOTIONAL DISTRESS (83 patients)
HYPOAESTHESIA (83 patients)
DECREASED APPETITE (82 patients)
DIABETES MELLITUS (81 patients)
DRUG EXPOSURE DURING PREGNANCY (80 patients)
CONFUSIONAL STATE (80 patients)
NECK PAIN (79 patients)
BRONCHOSPASM (79 patients)
DYSPNOEA EXERTIONAL (78 patients)
DYSGEUSIA (78 patients)
PARAESTHESIA (77 patients)
HYPERHIDROSIS (76 patients)
OSTEOARTHRITIS (75 patients)
GAIT DISTURBANCE (74 patients)
THERAPEUTIC RESPONSE DECREASED (74 patients)
URTICARIA (74 patients)
HYPOKALAEMIA (73 patients)
DRUG INTERACTION (73 patients)
ERYTHEMA (72 patients)
DEHYDRATION (72 patients)
RESPIRATORY ARREST (72 patients)
STATUS ASTHMATICUS (71 patients)
DYSPEPSIA (71 patients)
ABDOMINAL PAIN UPPER (70 patients)
PRODUCTIVE COUGH (70 patients)
CANDIDIASIS (70 patients)
NERVOUSNESS (68 patients)
PULMONARY EMBOLISM (68 patients)
ARRHYTHMIA (68 patients)
OSTEONECROSIS OF JAW (67 patients)
ANHEDONIA (67 patients)
RESPIRATORY DISTRESS (67 patients)
CYANOSIS (66 patients)
MUSCULAR WEAKNESS (64 patients)
DEEP VEIN THROMBOSIS (64 patients)
ATELECTASIS (63 patients)
CONTUSION (63 patients)
DYSPHAGIA (62 patients)
GENERAL PHYSICAL HEALTH DETERIORATION (62 patients)
BLOOD GLUCOSE INCREASED (62 patients)
OSTEOPENIA (61 patients)
OSTEOPOROSIS (61 patients)
HYPONATRAEMIA (60 patients)
CELLULITIS (59 patients)
ANOREXIA (58 patients)
ARTHROPATHY (58 patients)
CARDIAC FAILURE (58 patients)
OVERDOSE (58 patients)
STAPHYLOCOCCAL INFECTION (57 patients)
OSTEONECROSIS (57 patients)
ORAL CANDIDIASIS (57 patients)
HAEMOPTYSIS (57 patients)
SYNCOPE (56 patients)
CHILLS (56 patients)
DYSURIA (55 patients)
ABDOMINAL DISTENSION (54 patients)
CARDIOMEGALY (54 patients)
CATARACT (54 patients)
PULMONARY FIBROSIS (54 patients)
ANGINA PECTORIS (54 patients)
INFECTION (53 patients)
ASPARTATE AMINOTRANSFERASE INCREASED (53 patients)
ALOPECIA (52 patients)
PLEURAL EFFUSION (52 patients)
SWELLING (52 patients)
HYPERKALAEMIA (52 patients)
WHITE BLOOD CELL COUNT INCREASED (51 patients)
COLONIC POLYP (51 patients)
COMA (51 patients)
TRANSIENT ISCHAEMIC ATTACK (50 patients)
JOINT SWELLING (50 patients)
VISUAL ACUITY REDUCED (50 patients)
ILL-DEFINED DISORDER (50 patients)
CHOLELITHIASIS (50 patients)
NEUROPATHY PERIPHERAL (50 patients)
INTERSTITIAL LUNG DISEASE (49 patients)
NASOPHARYNGITIS (49 patients)
HYPOXIA (49 patients)
LIVER DISORDER (49 patients)
LUNG INFILTRATION (49 patients)
ABDOMINAL DISCOMFORT (48 patients)
INTERVERTEBRAL DISC DEGENERATION (48 patients)
ROTATOR CUFF SYNDROME (48 patients)
ALANINE AMINOTRANSFERASE INCREASED (48 patients)
DRUG WITHDRAWAL SYNDROME (48 patients)
DRUG HYPERSENSITIVITY (47 patients)
MENTAL DISORDER (47 patients)
DEPRESSED LEVEL OF CONSCIOUSNESS (47 patients)
BLOOD CHOLESTEROL INCREASED (47 patients)
BRADYCARDIA (47 patients)
ORAL PAIN (46 patients)
HEPATIC FUNCTION ABNORMAL (46 patients)
HAEMORRHAGE (46 patients)
URINARY INCONTINENCE (46 patients)
HAEMOGLOBIN DECREASED (45 patients)
SPINAL OSTEOARTHRITIS (45 patients)
AGITATION (45 patients)
SLEEP APNOEA SYNDROME (45 patients)
LUNG NEOPLASM (45 patients)
LUNG HYPERINFLATION (44 patients)
GASTRITIS (44 patients)
FEELING JITTERY (44 patients)
ACUTE MYOCARDIAL INFARCTION (43 patients)
EPISTAXIS (43 patients)
HOARSENESS (43 patients)
APHONIA (43 patients)
STRESS (43 patients)
ABSCESS (42 patients)
MEMORY IMPAIRMENT (42 patients)
LUNG DISORDER (42 patients)
TENDON RUPTURE (42 patients)
BLOOD PRESSURE DECREASED (42 patients)
RESPIRATORY DISORDER (42 patients)
CARDIAC DISORDER (41 patients)
ACUTE RESPIRATORY FAILURE (41 patients)
INTERVERTEBRAL DISC PROTRUSION (41 patients)
DIVERTICULITIS (41 patients)
DRUG DEPENDENCE (41 patients)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED (41 patients)
OSTEOMYELITIS (40 patients)
STOMATITIS (40 patients)
INCREASED UPPER AIRWAY SECRETION (40 patients)
SLEEP DISORDER (40 patients)
PLATELET COUNT DECREASED (40 patients)
POLLAKIURIA (39 patients)
MUSCULOSKELETAL PAIN (39 patients)
PNEUMOTHORAX (39 patients)
RIB FRACTURE (39 patients)
SWELLING FACE (39 patients)
URINARY RETENTION (39 patients)
ARTHRITIS (39 patients)
OEDEMA (38 patients)
PNEUMONITIS (38 patients)
MITRAL VALVE INCOMPETENCE (38 patients)
ECONOMIC PROBLEM (38 patients)

In addition to reviewing our up-to-date FDA research, users may interact with the FactMed community - currently one million members and growing! FactMed online research and discussions are read by patients, scientists, physicians, and other interested health care parties. Post follow up Questions to learn from our diverse readership. Likewise, patients who have experienced unwanted effects are encouraged to share their Concerns to help educate and inform our members.


Recent FactMed Activity for SEREVENT


Issue Description / Topic Timestamp
QUESTION
ARTHRALGIA
I had used Serevent for 18/19 days by 29 March 2014, and began to feel unwell. By April 7th began a course of Cephalexin for kidney pain. By May 6th almost unable to move with severe pain. Hips, knees, neck then shoulders and arm. Continued day and night for about 8 months. Now right hip very painful but on severe constant hot pain. CRP was 12 at one point but came down to 6. Was this post viral or a bad drug reaction. I am female aged 67 intolerant of asprin, anti inflammatories and calcium supplements. I am hypothyroid - take 50mg per day and have osteoporosis but take no drugs due to intolerance. 2015-02-25 15:53:25

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