BLOOD GLUCOSE DECREASED side effect
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Drugs associated with BLOOD GLUCOSE DECREASED
ABREVA ACCUTANE ACETAMINOPHEN ACETAZOLAMIDE ACIPHEX ACTOPLUS ACTOS ADALIMUMAB ADVAIR AERIUS ALEVE ALTACE AMARYL AMBIEN AMEVIVE AMIODARONE APIDRA ARIMIDEX ASPIRIN ATENOLOL ATRIPLA AUGMENTIN AVANDAMET AVANDARYL AVANDIA AVELOX AVODART AVONEX BACTRIM BENADRYL BETAMETHASONE BETASERON BOKEY BONIVA BORTEZOMIB BYETTA CAP CAPECITABINE CELEBREX CHAMPIX CHANTIX CIALIS CISPLATIN CLARITIN CLINDAMYCIN CLOZAPINE CLOZARIL COMBIVIR COREG CORGARD COZAAR CRANBERRY CRESTOR CYMBALTA CYTARABINE DEFINITY DERMA DETROL DEXAMETHASONE DEXTROAMPHETAMIN DEXTROSE DIANEAL DIGITEK DIGOXIN DILTIAZEM DIOVAN DIPHENHYDRAMINE DMPS DOCETAXEL DOXYCYCLINE DUETACT DURAGESIC EFFEXOR EMSAM ENABLEX ENBREL ERLOTINIB ESCITALOPRAM EXENATIDE EXTRANEAL EXUBERA FABRAZYME FACTIVE FASLODEX FENTANYL FENTORA FERROUS FLOMAX FLUCONAZOLE FORTAMET FORTEO GALVUS GATIFLO GLEEVEC GLIMEPIRIDE GLIPIZIDE GLUCOPHAGE GLUCOTROL GLUCOVANCE GLYBURIDE GUAIFENESIN HALDOL HEPARIN HUMALOG HUMIRA HUMULIN HYDROCHLOROTHIAZ HYDROCODONE IBUPROFEN ILETIN IMMUCYST IMMUNE IMODIUM INSULIN INTRON IRESSA JANUVIA LAMISIL LAMOTRIGINE LANTRISUL LANTUS LETAIRIS LEVAQUIN LEVEMIR LEVOFLOXACIN LEXAPRO LIORESAL LIPITOR LITHIUM LORAZEPAM LOVAZA LYRICA MERCAPTOPURINE MERIDIA METFORMIN METHOTREXATE METHYLPHENIDATE METOPROLOL MICRONASE MIRAPEX MIRENA MIRTAZAPINE MORPHINE NAMENDA NARDIL NATALIZUMAB NEURONTIN NEXAVAR NEXIUM NICARDIPINE NICOTINE NIQUITIN NORDITROPIN NORVASC NOVOLIN NOVOLOG NOVORAPID NPH NUTROPIN OCTAGAM OLANZAPINE OLMESARTAN OMEPRAZOLE OMNICEF ONE ORENCIA ORLISTAT OXYCODONE OXYCONTIN PAXIL PENFILL PENMIX PHENYTOIN PLAN PRECOSE PRINIVIL PROCARDIA PROCRIT PROGRAF PROVIGIL RANEXA REBIF REGULAR REMICADE REMINYL REPAGLANIDE REPREVE REQUIP REVACIZUMAB REVLIMID RIFADIN RIMACTANE RISPERDAL ROBITUSSIN ROSIGLITAZONE ROZEREM SANDOSTATIN SERETIDE SEROQUEL SIMVASTATIN SOMATROPIN SPIRIVA STALEVO STRATTERA SUBOXONE SUTENT SYMLIN SYMLINPEN SYNTHROID TARCEVA TAVOR TEGRETOL TEKTURNA THERAFLU TOPAMAX TOTAL TRACLEER TRICOR TYKERB TYLENOL TYSABRI VENTAVIS VERAPAMIL VESICARE VESLCARE VITAMIN VOLTAREN WELLBUTRIN XANAX XENICAL ZANTAC ZELNORM ZEMPLAR ZEVALIN ZIDOVUDINE ZINACEF ZOCOR ZYPREXA ZYVOXDianeal Side Effects Report #5647491-6
Health Professional from UNITED STATES reported DIANEAL problem on Feb 21, 2008. Male patient, 59 years of age, was diagnosed with peritoneal dialysis and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, catheter site erythema, pancreatitis, . DIANEAL dosage: unknown. During the same period patient was treated with PHOSLO, SENSIPAR, LYRICA, HYZAAR, LASIX, ALTACE, AMARYL, LANTUS. Patient was hospitalized. Patient recovered.
Exubera Side Effects Report #5649561-5
EXUBERA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, weighting 212.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXUBERA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, dyspnoea, wheezing, . EXUBERA dosage: unknown. During the same period patient was treated with BYETTA, ACTOS, ALPRAZOLAM, LEXAPRO, ECOTRIN, FOLTX, SYNTHROID, PREMARIN. Patient recovered.
Fentanyl Side Effects Report #5652492-8
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 25, 2008. Female patient, weighting 250.0 lb, was diagnosed with pain, nervousness, sleep disorder, muscle disorder, diabetes mellitus and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, confusional state, malaise, myalgia, nervousness, overdose, pain, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, XANAX, VICODIN, TRAZODONE, NORFLEX, NOVOLOG, COZAAR, METANX. Patient recovered.
Penmix Side Effects Report #5653019-7
PENMIX problem was reported by a Consumer or non-health professional from NEW ZEALAND on Feb 14, 2008. Female patient, 85 years of age, was treated with PENMIX. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, neoplasm malignant, . PENMIX dosage: unknown. Patient was hospitalized. Patient recovered.
Chantix Side Effects Report #5653884-3
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Feb 25, 2008. Female patient, weighting 172.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, blood magnesium decreased, loss of consciousness, neoplasm, oral surgery, . CHANTIX dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ACIPHEX, LANTUS, HUMALOG, PRAVACHOL, UNITHROID, METOCLOPRAMIDE, ZETIA. Patient was hospitalized. Patient recovered.
Strattera Side Effects Report #5653908-3
STRATTERA problem was reported by a Physician from UNITED STATES on Feb 26, 2008. Female patient, child 6 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, chest pain, . STRATTERA dosage: unknown. Patient recovered.
Byetta Side Effects Report #5655485-X
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Feb 26, 2008. Female patient, weighting 180.0 lb, was diagnosed with glaucoma and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, decreased appetite, eye discharge, eye haemorrhage, increased appetite, nausea, vision blurred, . BYETTA dosage: unknown. During the same period patient was treated with COSOPT, LUMIGAN, HUMALOG. Patient recovered.
Humalog Side Effects Report #5655493-9
HUMALOG problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Male patient was diagnosed with diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, cardiac disorder, tremor, weight increased, . HUMALOG dosage: unknown. During the same period patient was treated with HUMULIN, HUMULIN N. Patient was hospitalized. Patient recovered.
Aleve Side Effects Report #5656273-0
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Oct 11, 2007. Male patient, 68 years of age, weighting 169.8 lb, was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with INSULIN, SINGULAIR, SYNTHROID. Patient recovered.
Vitamin Side Effects Report #5656702-2
VITAMIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2008. Female patient, 61 years of age, weighting 170.0 lb, was treated with VITAMIN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, . VITAMIN dosage: unknown. During the same period patient was treated with ASPIRIN, FORADIL, SPIRIVA, SEREVENT, ALBUTEROL, CALCIUM, METFORMIN, SIMVASTATIN. Patient recovered.
Capecitabine Side Effects Report #5657230-0
Physician from UNITED STATES reported CAPECITABINE problem on Mar 07, 2008. Female patient, weighting 187.0 lb, was diagnosed with breast cancer and was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood lactic acid increased, blood pressure increased, body temperature decreased, cardiac arrest, diarrhoea, dysarthria, dyspnoea, heart rate increased, . CAPECITABINE dosage: 1650 MG BID ORALLY. Patient died on 03/03/2008.
Forteo Side Effects Report #5657629-2
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Male patient, 79 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, dizziness, implantable defibrillator insertion, loss of consciousness, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.
Vitamin Side Effects Report #5664393-X
Consumer or non-health professional from UNITED STATES reported VITAMIN problem on Feb 11, 2008. Female patient, 61 years of age, weighting 170.0 lb, was treated with VITAMIN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, . VITAMIN dosage: unknown. During the same period patient was treated with ASPIRIN, FORADIL, SPIRIVA, SEREVENT, ALBUTEROL, CALCIUM, METFORMIN, SIMVASTATIN. Patient recovered.
Heparin Side Effects Report #5664752-5
HEPARIN problem was reported by a Health Professional from UNITED STATES on Mar 07, 2008. Female patient, 69 years of age, was diagnosed with thrombosis, haemodialysis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood pressure decreased, dyspnoea, oedema peripheral, pneumonia, swelling face, thrombosis, . HEPARIN dosage: unknown. Patient was hospitalized. Patient died on 02/14/2008.
Novolog Side Effects Report #5669001-X
Health Professional from UNITED STATES reported NOVOLOG problem on Mar 06, 2008. Female patient, 23 years of age, was diagnosed with type 1 diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, intentional overdose, suicide attempt, . NOVOLOG dosage: unknown. During the same period patient was treated with LANTUS. Patient was hospitalized. Patient recovered.
Byetta Side Effects Report #5671095-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, eating disorder, knee arthroplasty, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with AVANDIA, PREVACID, CELEBREX. Patient was hospitalized. Patient recovered.
Dextrose Side Effects Report #5671662-6
Pharmacist from UNITED STATES reported DEXTROSE problem on Mar 06, 2008. Female patient, weighting 2.20 lb, was treated with DEXTROSE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, . DEXTROSE dosage: unknown. Patient recovered.
Altace Side Effects Report #5672793-7
ALTACE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 01, 2007. Female patient was diagnosed with hypertension, gastrooesophageal reflux disease and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood pressure increased, feeling abnormal, headache, . ALTACE dosage: 2.5 MG, QD. During the same period patient was treated with DILTIAZEM, FUROSEMIDE, PEPCID COMPLETE. Patient recovered.
Lorazepam Side Effects Report #5673078-5
Physician from JAPAN reported LORAZEPAM problem on Feb 28, 2008. Male patient, 63 years of age, was diagnosed with hypothyroidism, type 2 diabetes mellitus and was treated with LORAZEPAM. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, suicide attempt, thyroid function test abnormal, . LORAZEPAM dosage: (10 MG). During the same period patient was treated with LEVOTHYROXINE, GLIBENCLAMIDE, GLYBURIDE. Patient was hospitalized. Patient recovered.
Avandaryl Side Effects Report #5675465-8
AVANDARYL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 21, 2007. Female patient, 52 years of age, was treated with AVANDARYL. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, confusional state, hyperhidrosis, palpitations, . AVANDARYL dosage: unknown. During the same period patient was treated with ALTACE. Patient recovered.
Symlin Side Effects Report #5675834-6
Consumer or non-health professional from UNITED STATES reported SYMLIN problem on Mar 03, 2008. Female patient, 40 years of age, was diagnosed with type 1 diabetes mellitus and was treated with SYMLIN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, confusional state, treatment noncompliance, . SYMLIN dosage: unknown. During the same period patient was treated with HUMALOG, ORAL CONTRACEPTIVE NOS. Patient recovered.
Nexavar Side Effects Report #5676126-1
NEXAVAR problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2008. Male patient, 76 years of age, was diagnosed with hepatic neoplasm malignant, hypertension, hypercholesterolaemia, cardiovascular event prophylaxis, vitamin supplementation, diabetes mellitus and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, diarrhoea, epistaxis, oral pain, pain of skin, skin burning sensation, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with AVAPRO, ZETIA, TOPROL, ALLOPURINOL, ASPIRIN, NIACIN, GLYBURIDE. Patient was hospitalized. Patient recovered.
Heparin Side Effects Report #5676170-4
Health Professional from UNITED STATES reported HEPARIN problem on Mar 14, 2008. Female patient, 69 years of age, was diagnosed with thrombosis, haemodialysis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood pressure decreased, dyspnoea, oedema peripheral, pneumonia, swelling face, thrombosis, . HEPARIN dosage: unknown. Patient was hospitalized. Patient died on 02/14/2008.
Mirena Side Effects Report #5678453-0
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 19, 2008. Female patient, 43 years of age, weighting 251.3 lb, was diagnosed with hyperplasia and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, chest pain, depression, heart rate increased, pain in extremity, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.
Regular Side Effects Report #5682260-2
Pharmacist from UNITED STATES reported REGULAR INSULIN U problem on Mar 26, 2008. Female patient, 65 years of age, weighting 295.4 lb, was diagnosed with diabetes mellitus and was treated with REGULAR INSULIN U. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, fall, loss of consciousness, obesity, oedema peripheral, unresponsive to stimuli, urinary incontinence, . REGULAR INSULIN U dosage: unknown. During the same period patient was treated with REGULAR INSULIN U. Patient was hospitalized. Patient recovered.
Orencia Side Effects Report #5682527-8
ORENCIA problem was reported by a Health Professional from UNITED STATES on Dec 13, 2007. Male patient, 64 years of age, weighting 244.7 lb, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, . ORENCIA dosage: unknown. During the same period patient was treated with HUMALOG, AMARYL, PROTONIX, LISINOPRIL, AGGRENOX, DYAZIDE, LEXAPRO, PREDNISONE. Patient recovered.
Insulin Side Effects Report #5682702-2
Pharmacist from UNITED STATES reported INSULIN problem on Mar 26, 2008. Male patient, 47 years of age, was diagnosed with type 2 diabetes mellitus and was treated with INSULIN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, fatigue, hyperhidrosis, tremor, . INSULIN dosage: unknown. During the same period patient was treated with AUGMENTIN, LOMOTIL, METOPROLOL TARTRATE, NICOTINE, PSYLLIUM, ENOXAPARIN. Patient recovered.
Byetta Side Effects Report #5683138-0
BYETTA problem was reported by a Physician from RUSSIAN FEDERATION on Mar 20, 2008. Female patient, 45 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, hypoglycaemia, loss of consciousness, nausea, vomiting, . BYETTA dosage: unknown. During the same period patient was treated with SIOFOR, GLIBOMET. Patient recovered.
Symlinpen Side Effects Report #5683160-4
Consumer or non-health professional from UNITED STATES reported SYMLINPEN problem on Mar 13, 2008. Male patient, 87 years of age, was diagnosed with type 2 diabetes mellitus and was treated with SYMLINPEN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, . SYMLINPEN dosage: unknown. During the same period patient was treated with REGULAR INSULIN, HUMULIN N. Patient was hospitalized. Patient recovered.
Actoplus Side Effects Report #5683454-2
ACTOPLUS MET problem was reported by a Pharmacist from UNITED STATES on Mar 14, 2008. Female patient, 54 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOPLUS MET. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, incorrect dose administered, . ACTOPLUS MET dosage: 15 MG/850 MG, 2 IN 1 D, PER ORAL; 15 MG/500 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with ACTOPLUS MET. Patient recovered.
Avelox Side Effects Report #5685466-1
Consumer or non-health professional from UNITED STATES reported AVELOX problem on Feb 26, 2008. Male patient, 60 years of age, was diagnosed with infection prophylaxis, diabetes mellitus and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, confusional state, depressed level of consciousness, mental impairment, . AVELOX dosage: unknown. During the same period patient was treated with DOXYCYCLINE, SEPTRA, SYMLIN, HUMALOG, LANTUS, BYETTA. Patient recovered.
Novolog Side Effects Report #5688846-3
NOVOLOG problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 25, 2008. Male patient, 55 years of age, was diagnosed with type 1 diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, contusion, fall, loss of consciousness, . NOVOLOG dosage: unknown. During the same period patient was treated with NOVOLIN N. Patient recovered.
Corgard Side Effects Report #5689167-5
Consumer or non-health professional from UNITED KINGDOM reported CORGARD problem on Mar 27, 2008. Female patient was diagnosed with long qt syndrome and was treated with CORGARD. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, hypoglycaemic seizure, . CORGARD dosage: 20 MG, UNK. Patient recovered.
Lyrica Side Effects Report #5689499-0
LYRICA problem was reported by a Physician from UNITED STATES on Mar 19, 2008. Male patient, 49 years of age, was diagnosed with neck pain, back pain and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, coma, dyspnoea, lethargy, pyrexia, renal failure, rhabdomyolysis, septic shock, . LYRICA dosage: unknown. During the same period patient was treated with CHOLESTEROL. Patient was hospitalized. Patient died.
Theraflu Side Effects Report #5691304-3
Consumer or non-health professional from UNITED STATES reported THERAFLU COLD AND COUGH problem on Mar 13, 2008. Female patient, 34 years of age, was treated with THERAFLU COLD AND COUGH. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, fall, influenza, musculoskeletal disorder, . THERAFLU COLD AND COUGH dosage: unknown. During the same period patient was treated with GLUCOPHAGE. Patient recovered.
Lovaza Side Effects Report #5691318-3
LOVAZA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 18, 2008. Female patient was treated with LOVAZA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, . LOVAZA dosage: unknown. Patient recovered.
Fentora Side Effects Report #5691488-7
Physician from UNITED STATES reported FENTORA problem on Mar 17, 2008. Male patient, 82 years of age, weighting 255.0 lb, was diagnosed with pain and was treated with FENTORA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, insomnia, tremor, . FENTORA dosage: unknown. During the same period patient was treated with MORPHINE. Patient recovered.
Fentanyl Side Effects Report #5610566-1
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2008. Female patient, weighting 133.0 lb, was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, somnolence, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM. Patient recovered.
Apidra Side Effects Report #5611073-2
Consumer or non-health professional from UNITED STATES reported APIDRA problem on Jan 23, 2008. Female patient, 53 years of age, was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, hyperglycaemia, thrombosis, . APIDRA dosage: unknown. During the same period patient was treated with OPTICLIK, LANTUS, COREG, BETA PROPRANOLOL, PROTONIX, ALDACTONE. Patient was hospitalized. Patient recovered.
Humulin Side Effects Report #5611431-6
HUMULIN N problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2008. Male patient was treated with HUMULIN N. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, fall, femur fracture, . HUMULIN N dosage: unknown. During the same period patient was treated with HUMULIN R, LANTUS. Patient was hospitalized. Patient recovered.
Humulin Side Effects Report #5611451-1
Consumer or non-health professional from UNITED STATES reported HUMULIN R problem on Jan 21, 2008. Male patient was treated with HUMULIN R. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, dialysis, . HUMULIN R dosage: unknown. During the same period patient was treated with HUMULIN N, HUMULIN N. Patient recovered.
Reminyl Side Effects Report #5613913-X
REMINYL problem was reported by a Health Professional from UNITED KINGDOM on Jan 25, 2008. Male patient, 73 years of age, was diagnosed with dementia and was treated with REMINYL. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, . REMINYL dosage: unknown. Patient recovered.
Humulin Side Effects Report #5614734-4
Consumer or non-health professional from UNITED STATES reported HUMULIN N problem on Jan 25, 2008. Male patient, 63 years of age, was diagnosed with diabetes mellitus and was treated with HUMULIN N. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, cerebrovascular accident, . HUMULIN N dosage: unknown. Patient was hospitalized. Patient recovered.
Humulin Side Effects Report #5614742-3
HUMULIN N problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 28, 2008. Female patient was treated with HUMULIN N. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood glucose increased, cataract, dizziness, gait disturbance, gastric disorder, gastric ulcer, hospitalisation, . HUMULIN N dosage: unknown. During the same period patient was treated with HUMULIN N, HUMULIN R, HUMULIN R, NPH ILETIN I, INSULIN, CORTISONE, PREDNISONE. Patient was hospitalized. Patient recovered.
Humulin Side Effects Report #5614749-6
Consumer or non-health professional from UNITED STATES reported HUMULIN R problem on Jan 28, 2008. Male patient was treated with HUMULIN R. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, dialysis, loss of consciousness, . HUMULIN R dosage: unknown. During the same period patient was treated with HUMULIN N, HUMULIN N. Patient was hospitalized. Patient recovered.
Mirena Side Effects Report #5614901-X
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 24, 2008. Female patient, 43 years of age, weighting 251.3 lb, was diagnosed with hyperplasia and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, chest pain, depression, heart rate increased, pain in extremity, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.
Lantus Side Effects Report #5615424-4
Consumer or non-health professional from AUSTRALIA reported LANTUS problem on Jan 30, 2008. Female patient, 72 years of age, was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, myocardial infarction, . LANTUS dosage: unknown. Patient was hospitalized. Patient recovered.
Exubera Side Effects Report #5615923-5
EXUBERA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 28, 2008. Male patient, weighting 188.1 lb, was treated with EXUBERA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, loss of consciousness, unresponsive to stimuli, . EXUBERA dosage: TEXT:3 MG. During the same period patient was treated with PROPRANOLOL, ENULOSE, LEXAPRO, NEOMYCIN, SPIRONOLACTONE, FUROSEMIDE, VITAMIN D, MORPHINE SULPHATE. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5616696-2
Consumer or non-health professional from UNITED STATES reported DIOVAN problem on Jan 30, 2008. Male patient was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, electrolyte imbalance, loss of consciousness, . DIOVAN dosage: 320 MG, UNK. Patient was hospitalized. Patient recovered.
Lantus Side Effects Report #5618370-5
LANTUS problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 31, 2008. Female patient, weighting 120.2 lb, was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood potassium increased, depressed level of consciousness, diabetes mellitus inadequate control, diabetic retinopathy, hyperglycaemia, hypoglycaemia, muscle twitching, pneumonia, . LANTUS dosage: unknown. During the same period patient was treated with HUMALOG, TOBRAXIA, SYNTHROID. Patient was hospitalized. Patient recovered.
Cymbalta Side Effects Report #5618898-8
Consumer or non-health professional from IRELAND reported CYMBALTA problem on Jan 28, 2008. Male patient, 34 years of age, was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, . CYMBALTA dosage: 30 MG, DAILY (1/D) FOR TWO WEEKS. During the same period patient was treated with INSULIN. Patient recovered.