Is FLUSHING a side effect of ALBUMINAR-25 ? ( FactMed.com )

 

About this FactMed analysis covering adverse side effect reports of ALBUMINAR-25 patients who developed FLUSHING.

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 ALBUMINAR-25 reported FLUSHING to the FDA. A total of 49 ALBUMINAR-25 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 ALBUMINAR-25 and FLUSHING. In doing so, we compare ALBUMINAR-25 with other drugs that cause FLUSHING, to help you evaluate whether or not ALBUMINAR-25 causes FLUSHING. Likewise, this page shows the most highly-reported side effects of ALBUMINAR-25, so you can see if FLUSHING ranks among ALBUMINAR-25's most well-known side effects.
Summary Statistics
Reports of ALBUMINAR-25 causing FLUSHING: 2
Reports of any side effect of ALBUMINAR-25 : 49
Percentage of ALBUMINAR-25 patients where FLUSHING is a reported side effect: 4.0816%

FDA reports of any drug causing FLUSHING : 34663
Average percentage for all medicated patients where FLUSHING is reported as a complication: 0.2172%

Physician opinion on ALBUMINAR-25 as adverse event culprit:

Overall opinion for all reports of this drug:
Most frequent diagnoses/indications for prescribing ALBUMINAR-25:
PRODUCT USED FOR UNKNOWN INDICATION ( 9 patients )
HYPOALBUMINAEMIA ( 6 patients )
CARDIAC FAILURE ( 2 patients )
SURGERY ( 2 patients )
DRUG USE FOR UNKNOWN INDICATION ( 2 patients )
HAEMODYNAMIC INSTABILITY ( 2 patients )
METASTASES TO LYMPH NODES ( 2 patients )
NEPHROTIC SYNDROME ( 2 patients )
RENAL FAILURE ACUTE ( 2 patients )
URINE OUTPUT DECREASED ( 2 patients )
HEPATIC CIRRHOSIS ( 2 patients )
HYPOTENSION ( 2 patients )
MYASTHENIA GRAVIS ( 1 patients )
PLASMAPHERESIS ( 1 patients )
LIVER DISORDER ( 1 patients )
PNEUMONIA ( 1 patients )
ASCITES ( 1 patients )
CENTRAL VENOUS PRESSURE DECREASED ( 1 patients )
GENERALISED OEDEMA ( 1 patients )
LYMPHANGIOMA ( 1 patients )
( 0 patients )
Drugs with high FDA adverse event association with FLUSHING:

NIASPAN (20887 patients)
ASPIRIN (9994 patients)
SIMCOR (6297 patients)
LISINOPRIL (2500 patients)
REMICADE (2315 patients)
FISH OIL (2167 patients)
CRESTOR (1793 patients)
LIPITOR (1760 patients)
SIMVASTATIN (1730 patients)
SANDOSTATIN LAR (1634 patients)
PLAVIX (1582 patients)
SYNTHROID (1044 patients)
ATENOLOL (1024 patients)
MULTI-VITAMIN (1010 patients)
HYDROCHLOROTHIAZIDE (972 patients)
VITAMIN D (970 patients)
METFORMIN HCL (946 patients)
LOVAZA (938 patients)
METOPROLOL TARTRATE (881 patients)
NEXIUM (848 patients)
OMEPRAZOLE (783 patients)
METOPROLOL (772 patients)
M.V.I. (757 patients)
LEVOTHYROXINE SODIUM (749 patients)
ACETYLSALICYLIC ACID SRT (718 patients)
BENADRYL (691 patients)
DIOVAN (666 patients)
CALCIUM (666 patients)
COUMADIN (661 patients)
HEPARIN SODIUM INJECTION (655 patients)
METFORMIN (639 patients)
FOLIC ACID (632 patients)
TOPROL-XL (626 patients)
PRILOSEC (621 patients)
IBUPROFEN (608 patients)
AMLODIPINE (607 patients)
ZETIA (605 patients)
TYSABRI (581 patients)
VIAGRA (558 patients)
ALLOPURINOL (541 patients)
TRICOR (525 patients)
FUROSEMIDE (513 patients)
ZOCOR (509 patients)
NORVASC (488 patients)
LASIX (476 patients)
ASCORBIC ACID (458 patients)
PREDNISONE (451 patients)
COREG (442 patients)
PRAVASTATIN (419 patients)
XANAX (417 patients)
METHOTREXATE (411 patients)
WARFARIN SODIUM (399 patients)
BENICAR (398 patients)
CARVEDILOL (393 patients)
LEVITRA (388 patients)
POTASSIUM CHLORIDE (384 patients)
HUMIRA (378 patients)
ACTOS (372 patients)
VYTORIN (370 patients)
SINGULAIR (367 patients)
LANTUS (364 patients)
VITAMIN B-12 (358 patients)
PROTONIX (357 patients)
ENBREL (356 patients)
TRILIPIX (355 patients)
RAMIPRIL (348 patients)
HEPARIN SODIUM (347 patients)
FOSAMAX (345 patients)
COATED PDS (344 patients)
PREVACID (342 patients)
DIGOXIN (341 patients)
LEXAPRO (341 patients)
MULTI-VITAMINS (338 patients)
ZOLOFT (333 patients)
COQ10 (332 patients)
ACETAMINOPHEN (329 patients)
GABAPENTIN (324 patients)
CELEBREX (317 patients)
DEXAMETHASONE (316 patients)
GLIPIZIDE (301 patients)
UNKNOWN MEDICATION (300 patients)
ALBUTEROL (294 patients)
FLOMAX (290 patients)
BYETTA (290 patients)
CYMBALTA (289 patients)
AMBIEN (287 patients)
MVT (285 patients)
LORAZEPAM (282 patients)
ZYRTEC (282 patients)
VIT D (282 patients)
FENOFIBRATE (282 patients)
DECADRON (276 patients)
PACLITAXEL (269 patients)
CARBOPLATIN (267 patients)
LYRICA (267 patients)
ADVAIR DISKUS 100/50 (267 patients)
ZANTAC (264 patients)
RANITIDINE (261 patients)
CIALIS (261 patients)
NEURONTIN (259 patients)
ADVICOR (255 patients)
LOVASTATIN (248 patients)
CLONAZEPAM (243 patients)
INSULIN (243 patients)
COZAAR (241 patients)
GLUCOSAMINE (240 patients)
ALLEGRA (237 patients)
VITAMIN E (234 patients)
NITROGLYCERIN (231 patients)
VIOXX (231 patients)
ALTACE (226 patients)
POTASSIUM (225 patients)
AVONEX (225 patients)
SPIRONOLACTONE (225 patients)
TRAZODONE HCL (224 patients)
NEXAVAR (224 patients)
FORTEO (222 patients)
GLUCOPHAGE (222 patients)
WELLBUTRIN (221 patients)
DIOVAN HCT (219 patients)
TRAMADOL HCL (219 patients)
GLYBURIDE (216 patients)
VICODIN (215 patients)
LEVOXYL (214 patients)
EFFEXOR (214 patients)
CLOPIDOGREL (214 patients)
SANDOSTATIN (212 patients)
METOPROLOL SUCCINATE (210 patients)
METFORMIN HYDROCHLORIDE (209 patients)
AVELOX (209 patients)
ATORVASTATIN CALCIUM (208 patients)
SOLU-MEDROL (206 patients)
VITAMIN B COMPLEX CAP (202 patients)
PAXIL (201 patients)
IRON (200 patients)
PREDNISOLONE (199 patients)
ATIVAN (198 patients)
VITAMIN TAB (196 patients)
PREMARIN (195 patients)
CLARITIN (191 patients)
SPIRIVA (188 patients)
BYSTOLIC (187 patients)
BLOOD PRESSURE MEDICATION (184 patients)
LOPRESSOR (182 patients)
SEROQUEL (179 patients)
LEVOTHYROXINE (179 patients)
JANUVIA (177 patients)
ALPRAZOLAM (177 patients)
CLONIDINE (176 patients)
MAGNESIUM (175 patients)
VIT C (174 patients)
WELCHOL (172 patients)
FLUOROURACIL (172 patients)
TAXOTERE (171 patients)
CELEXA (168 patients)
XOLAIR (168 patients)
MICARDIS (167 patients)
HYZAAR (166 patients)
TRACLEER (166 patients)
LOTREL (166 patients)
LOSARTAN POTASSIUM (165 patients)
NIACIN (164 patients)
PROZAC (164 patients)
FLONASE (163 patients)
DILTIAZEM (163 patients)
COPAXONE (163 patients)
ENALAPRIL MALEATE (162 patients)
VERAPAMIL (161 patients)
KLONOPIN (160 patients)
NAPROXEN (160 patients)
TYLENOL (159 patients)
ZOFRAN (158 patients)
PREDNISONE TAB (158 patients)
OXYCONTIN (158 patients)
AVAPRO (157 patients)
TYLENOL (CAPLET) (156 patients)
LANSOPRAZOLE (155 patients)
DOCETAXEL (154 patients)
SYMBICORT (151 patients)
MELOXICAM (150 patients)
ERBITUX (150 patients)
HYDROCORTISONE (149 patients)
TAXOL (149 patients)
VITAMINS (146 patients)
GLIMEPIRIDE (146 patients)
MAGNEVIST (145 patients)
UNKNOWN MEDICATIONS (145 patients)
LISINOPRIL AND HYDROCHLOROTHIAZIDE (145 patients)
CARDIZEM (144 patients)
DIAZEPAM (142 patients)
GEMFIBROZIL (137 patients)
AMITRIPTYLINE HCL (135 patients)
MORPHINE (135 patients)
LAMICTAL (133 patients)
SOLU-CORTEF (133 patients)
ACIPHEX (133 patients)
PERCOCET (132 patients)
CALCIUM ACETATE (132 patients)
IMITREX (129 patients)
PANTOPRAZOLE (129 patients)
FLEXERIL (127 patients)
PRAVACHOL (127 patients)
FLUOXETINE (127 patients)
CITALOPRAM HYDROBROMIDE (126 patients)
JANUMET (123 patients)
BENAZEPRIL HYDROCHLORIDE (122 patients)
TOPAMAX (122 patients)
ATACAND (121 patients)
DEFINITY (121 patients)
LORTAB (121 patients)
Most common side effects for patients taking ALBUMINAR-25:
BLOOD PRESSURE DECREASED (11 patients)
INFUSION RELATED REACTION (7 patients)
HEPATITIS C POSITIVE (4 patients)
OXYGEN SATURATION DECREASED (4 patients)
HEPATIC FAILURE (3 patients)
HEPATITIS C ANTIBODY POSITIVE (3 patients)
TACHYCARDIA (3 patients)
HEPATITIS C VIRUS TEST POSITIVE (3 patients)
ANTINUCLEAR ANTIBODY POSITIVE (3 patients)
PYREXIA (3 patients)
HYPERSENSITIVITY (3 patients)
CHILLS (3 patients)
BLOOD CULTURE POSITIVE (2 patients)
PLATELET COUNT DECREASED (2 patients)
LOSS OF CONSCIOUSNESS (2 patients)
PRODUCT QUALITY ISSUE (2 patients)
KLEBSIELLA INFECTION (2 patients)
BACTERIAL INFECTION (2 patients)
BODY TEMPERATURE INCREASED (2 patients)
HYPOXIA (2 patients)
HYPOTENSION (2 patients)
PRURITUS (2 patients)
PULMONARY EMBOLISM (2 patients)
RASH (2 patients)
HEPATITIS C RNA POSITIVE (2 patients)
CROHN'S DISEASE (2 patients)
RESTLESSNESS (2 patients)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT (2 patients)
HEPATITIS B VIRUS TEST POSITIVE (2 patients)
HEPATITIS B POSITIVE (2 patients)
DYSKINESIA (2 patients)
HEPATITIS (2 patients)
HEPATITIS C (2 patients)
HEADACHE (2 patients)
FOAMING AT MOUTH (2 patients)
FLUSHING (2 patients)
FATIGUE (1 patients)
HAEMOGLOBIN DECREASED (1 patients)
HAEMOLYSIS (1 patients)
EYE SWELLING (1 patients)
ENTEROCOLONIC FISTULA (1 patients)
HEPATIC FUNCTION ABNORMAL (1 patients)
DYSPNOEA (1 patients)
HEPATITIS B CORE ANTIGEN POSITIVE (1 patients)
DRUG HYPERSENSITIVITY (1 patients)
HEPATITIS B SURFACE ANTIGEN POSITIVE (1 patients)
DIARRHOEA (1 patients)
ABDOMINAL DISCOMFORT (1 patients)
CYANOSIS (1 patients)
CULTURE URINE POSITIVE (1 patients)
CORONARY ARTERY INSUFFICIENCY (1 patients)
COOMBS DIRECT TEST POSITIVE (1 patients)
COMPLICATIONS OF TRANSPLANTED LIVER (1 patients)
CATHETER SITE HAEMORRHAGE (1 patients)
CARDIO-RESPIRATORY ARREST (1 patients)
BLOOD PRESSURE SYSTOLIC DECREASED (1 patients)
INTERNATIONAL NORMALISED RATIO INCREASED (1 patients)
BLOOD PRESSURE FLUCTUATION (1 patients)
LABORATORY TEST ABNORMAL (1 patients)
LARGE INTESTINE PERFORATION (1 patients)
LIP SWELLING (1 patients)
LIVER TRANSPLANT (1 patients)
BLOOD GLUCOSE INCREASED (1 patients)
NEUTROPHIL COUNT DECREASED (1 patients)
NOSOCOMIAL INFECTION (1 patients)
ORTHOPNOEA (1 patients)
BLOOD FIBRINOGEN DECREASED (1 patients)
PALLOR (1 patients)
BLOOD CREATININE INCREASED (1 patients)
PNEUMONIA KLEBSIELLA (1 patients)
POST PROCEDURAL COMPLICATION (1 patients)
PRODUCT OUTER PACKAGING ISSUE (1 patients)
PRODUCT PACKAGING QUANTITY ISSUE (1 patients)
BLOOD BILIRUBIN INCREASED (1 patients)
PROTHROMBIN TIME PROLONGED (1 patients)
BACK PAIN (1 patients)
ASTHENIA (1 patients)
PULMONARY OEDEMA (1 patients)
ASPARTATE AMINOTRANSFERASE INCREASED (1 patients)
ANAPHYLACTIC SHOCK (1 patients)
RECTAL HAEMORRHAGE (1 patients)
RENAL DISORDER (1 patients)
ANAPHYLACTIC REACTION (1 patients)
RETROPERITONEAL ABSCESS (1 patients)
SEROLOGY POSITIVE (1 patients)
SWELLING FACE (1 patients)
ALANINE AMINOTRANSFERASE INCREASED (1 patients)
ADVERSE EVENT (1 patients)
UPPER GASTROINTESTINAL HAEMORRHAGE (1 patients)
URINARY TRACT INFECTION FUNGAL (1 patients)
URINE OUTPUT DECREASED (1 patients)
URTICARIA (1 patients)
VENA CAVA THROMBOSIS (1 patients)
WHITE BLOOD CELL COUNT DECREASED (1 patients)

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