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DIZZINESS ( 20 FDA reports)
FATIGUE ( 20 FDA reports)
PALPITATIONS ( 20 FDA reports)
DYSPNOEA ( 17 FDA reports)
DEPRESSION ( 16 FDA reports)
ARTHRALGIA ( 14 FDA reports)
PAIN ( 14 FDA reports)
NAUSEA ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
ASTHENIA ( 12 FDA reports)
CONSTIPATION ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
COUGH ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
RASH ( 9 FDA reports)
VISUAL ACUITY REDUCED ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
CYST ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
INJURY ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
LOCAL SWELLING ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
OSTEOPENIA ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
THYROID DISORDER ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ACUTE STRESS DISORDER ( 6 FDA reports)
ANAL INFLAMMATION ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
ATELECTASIS ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
BREAST OPERATION ( 6 FDA reports)
BREAST RECONSTRUCTION ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CERVICAL SPINAL STENOSIS ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DISABILITY ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
GALLBLADDER OPERATION ( 6 FDA reports)
HAEMORRHOIDS ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HOT FLUSH ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 6 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 6 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
KIDNEY INFECTION ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LOBAR PNEUMONIA ( 6 FDA reports)
LUNG NEOPLASM ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
METASTATIC NEOPLASM ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
OEDEMA MUCOSAL ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
PARANASAL SINUS DISCOMFORT ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
SKIN CYST EXCISION ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
VENOUS OCCLUSION ( 6 FDA reports)
VENOUS THROMBOSIS ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VITAMIN B12 DEFICIENCY ( 6 FDA reports)
VULVOVAGINAL DRYNESS ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
FALL ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NODULE ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
TREMOR ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD OESTROGEN INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXPOSURE TO CONTAMINATED DEVICE ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)

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