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BLOOD GLUCOSE INCREASED ( 199 FDA reports)
NAUSEA ( 185 FDA reports)
WEIGHT DECREASED ( 168 FDA reports)
DECREASED APPETITE ( 86 FDA reports)
BLOOD GLUCOSE DECREASED ( 85 FDA reports)
VOMITING ( 56 FDA reports)
DIARRHOEA ( 37 FDA reports)
HEADACHE ( 34 FDA reports)
DIZZINESS ( 30 FDA reports)
DYSPEPSIA ( 27 FDA reports)
INJECTION SITE BRUISING ( 27 FDA reports)
ANOREXIA ( 26 FDA reports)
DRUG INEFFECTIVE ( 24 FDA reports)
INJECTION SITE PAIN ( 22 FDA reports)
ASTHENIA ( 21 FDA reports)
FATIGUE ( 19 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 19 FDA reports)
TREMOR ( 19 FDA reports)
FEELING ABNORMAL ( 18 FDA reports)
INJECTION SITE HAEMORRHAGE ( 18 FDA reports)
MEDICATION ERROR ( 18 FDA reports)
ABDOMINAL DISTENSION ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 17 FDA reports)
FEELING JITTERY ( 16 FDA reports)
ERUCTATION ( 15 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 13 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
DRUG EFFECT DECREASED ( 12 FDA reports)
CHILLS ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
PAIN ( 10 FDA reports)
NERVOUSNESS ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
EARLY SATIETY ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
STRESS ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
ENERGY INCREASED ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INJECTION SITE NODULE ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INJECTION SITE EXTRAVASATION ( 4 FDA reports)
INJECTION SITE URTICARIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
SWELLING ( 4 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FALL ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
THIRST ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TENSION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)

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