Please choose an event type to view the corresponding MedsFacts report:

FATIGUE ( 33 FDA reports)
CHEST PAIN ( 32 FDA reports)
DEPRESSION ( 30 FDA reports)
CROHN'S DISEASE ( 27 FDA reports)
IRRITABLE BOWEL SYNDROME ( 25 FDA reports)
DIZZINESS ( 23 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 23 FDA reports)
VOMITING ( 23 FDA reports)
PAIN IN EXTREMITY ( 22 FDA reports)
HEADACHE ( 21 FDA reports)
INSOMNIA ( 21 FDA reports)
RASH ( 21 FDA reports)
DIARRHOEA ( 19 FDA reports)
EYE PAIN ( 19 FDA reports)
VISION BLURRED ( 19 FDA reports)
BLOOD PRESSURE INCREASED ( 18 FDA reports)
DISTURBANCE IN ATTENTION ( 18 FDA reports)
HYPOAESTHESIA ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
PHOTOPHOBIA ( 18 FDA reports)
VERTIGO ( 18 FDA reports)
ABDOMINAL PAIN ( 17 FDA reports)
AGITATION ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
AMNESIA ( 16 FDA reports)
ANXIETY DISORDER ( 16 FDA reports)
DISORIENTATION ( 16 FDA reports)
INNER EAR DISORDER ( 16 FDA reports)
MOOD SWINGS ( 16 FDA reports)
NERVOUSNESS ( 16 FDA reports)
NIGHT SWEATS ( 16 FDA reports)
NIGHTMARE ( 16 FDA reports)
NYSTAGMUS ( 16 FDA reports)
PAIN OF SKIN ( 16 FDA reports)
PHONOPHOBIA ( 16 FDA reports)
PSYCHOTIC DISORDER ( 16 FDA reports)
TESTICULAR PAIN ( 16 FDA reports)
TINNITUS ( 16 FDA reports)
VESTIBULAR DISORDER ( 16 FDA reports)
COAGULOPATHY ( 15 FDA reports)
COLITIS ULCERATIVE ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
HYPERTENSION ( 14 FDA reports)
ARTERIAL RESTENOSIS ( 13 FDA reports)
ARTHRALGIA ( 13 FDA reports)
BACK PAIN ( 13 FDA reports)
CELLULITIS ( 12 FDA reports)
MOUTH ULCERATION ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
OESOPHAGEAL ULCER ( 11 FDA reports)
CARDIAC DISORDER ( 10 FDA reports)
CHONDROPATHY ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
ILEITIS ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ANAL HAEMORRHAGE ( 9 FDA reports)
COLITIS ( 9 FDA reports)
COLON ADENOMA ( 9 FDA reports)
FLANK PAIN ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
MULTI-ORGAN DISORDER ( 9 FDA reports)
DEAFNESS ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
ULNAR NERVE PALSY ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
INFECTION ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
ACIDOSIS ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ACNE ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
CYANOSIS NEONATAL ( 5 FDA reports)
DEATH ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
PAIN ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SPUTUM INCREASED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ASTHMA ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
PILONIDAL CYST CONGENITAL ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SMALL FOR DATES BABY ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VAGINAL MYCOSIS ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
COUGH ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 3 FDA reports)
FALL ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STRESS ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANKLE IMPINGEMENT ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFLAMMATION LOCALISED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NEONATAL HYPOTENSION ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
RALES ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TETHERED CORD SYNDROME ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VIRAL LABYRINTHITIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BANKRUPTCY ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NODULE ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN COSMETIC PROCEDURE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)

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